83 FR 28774 - Extension of Compliance Dates for Medical Examiner's Certification Integration
DEPARTMENT OF TRANSPORTATION
Federal Motor Carrier Safety Administration Federal Register Volume 83, Issue 120 (June 21, 2018)
Federal Motor Carrier Safety Administration
Federal Register Volume 83, Issue 120 (June 21, 2018)
| Page Range | 28774-28783 | |
| FR Document | 2018-13314 |
[Federal Register Volume 83, Number 120 (Thursday, June 21, 2018)] [Rules and Regulations] [Pages 28774-28783] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-13314] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF TRANSPORTATION Federal Motor Carrier Safety Administration 49 CFR Parts 383, 384, and 391 [Docket No. FMCSA-2018-0152] RIN 2126-AC18 Extension of Compliance Dates for Medical Examiner's Certification Integration AGENCY: Federal Motor Carrier Safety Administration (FMCSA), DOT. ACTION: Interim final rule; request for comments. ----------------------------------------------------------------------- SUMMARY: FMCSA amends its regulations to delay the compliance date from June 22, 2018, to June 22, 2021, for several provisions of its April 23, 2015 Medical Examiner's Certification Integration final rule. This action is being taken to provide FMCSA additional time to complete certain information technology (IT) system development tasks for its National Registry of Certified Medical Examiners (National Registry) and provide the State Driver's Licensing Agencies (SDLAs) sufficient time to make the necessary IT programming changes after upgrades to the National Registry. DATES: Effective Date: This interim final rule is effective June 21, 2018. Public Comment Period: Comments must be received on or before August 20, 2018. ADDRESSES: You may submit comments identified by Docket Number FMCSA- 2018-0152 using any of the following methods:Federal eRulemaking Portal: http://www.regulations.gov. Follow the online instructions for submitting comments. Mail: Docket Management Facility, U.S. Department of Transportation, 1200 New Jersey Avenue SE, West Building, Ground Floor, Room W12-140, Washington, DC 20590-0001. Hand Delivery or Courier: West Building, Ground Floor, Room W12-140, 1200 New Jersey Avenue SE, Washington, DC, between 9 a.m. and 5 p.m., Monday through Friday, except Federal holidays. Fax: 202-493-2251. To avoid duplication, please use only one of these four methods. See the ``Public Participation and Request for Comments'' portion of the SUPPLEMENTARY INFORMATION section for instructions on submitting comments, including collection of information comments for the Office of Information and Regulatory Affairs, OMB. FOR FURTHER INFORMATION CONTACT: Ms. Christine A. Hydock, Chief, Medical Programs Division, Federal Motor Carrier Safety Administration, 1200 New Jersey Avenue SE, Washington, DC 20590-0001, by telephone at 202-366-4001, or by email at [email protected]. If you have questions on viewing or submitting material to the docket, contact Docket Services, telephone (202) 366-9826. SUPPLEMENTARY INFORMATION: I. Rulemaking Documents A. Submitting Comments If you submit a comment, please include the docket number for this interim final rule (Docket No. FMCSA-2018-0152), indicate the specific section of this document to which each comment applies, and provide a reason for each suggestion or recommendation. You may submit your comments and material online or by fax, mail, or hand delivery, but please use only one of these means. FMCSA recommends that you include your name and a mailing address, an email address, or a phone number in the body of your document so that FMCSA can contact you if there are questions regarding your submission. To submit your comment online, go to http://www.regulations.gov, put the docket number, FMCSA-2018-0152, in the keyword box, and click ``Search.'' When the new screen appears, click on the ``Comment Now!'' button and type your comment into the text box on the following screen. Choose whether you are submitting your comment as an individual or on behalf of a third party and then submit. If you submit your comments by mail or hand delivery, submit them in an unbound format, no larger than 8\1/2\ by 11 inches, suitable for copying and electronic filing. If you submit comments by mail and would like to know that they reached the facility, please enclose a stamped, self-addressed postcard or envelope. FMCSA will consider all comments and material received during the [[Page 28775]] comment period and may change this interim final rule based on your comments. FMCSA may issue a final rule at any time after the close of the comment period. Confidential Business Information Confidential Business Information (CBI) is commercial or financial information that is customarily not made available to the public by the submitter. Under the Freedom of Information Act, CBI is eligible for protection from public disclosure. If you have CBI that is relevant or responsive to this interim final rule it is important that you clearly designate the submitted comments as CBI. Accordingly, please mark each page of your submission as ``confidential'' or ``CBI.'' Submissions designated as CBI and meeting the definition noted above will not be placed in the public docket of this interim final rule. Submissions containing CBI should be sent to Mr. Brian Dahlin, Chief, Regulatory Evaluation Division, 1200 New Jersey Avenue SE, Washington, DC 20590. Any commentary that FMCSA receives that is not specifically designated as CBI will be placed in the public docket for this rulemaking. FMCSA will consider all comments and material received during the comment period. B. Viewing Comments and Documents To view comments, as well as any documents mentioned in this preamble as being available in the docket, go to http://www.regulations.gov. Insert the docket number, FMCSA-2018-0152, in the keyword box, and click ``Search.'' Next, click the ``Open Docket Folder'' button and choose the document to review. If you do not have access to the internet, you may view the docket online by visiting the Docket Management Facility in Room W12-140 on the ground floor of the DOT West Building, 1200 New Jersey Avenue SE, Washington, DC 20590, between 9 a.m. and 5 p.m., E.T., Monday through Friday, except Federal holidays. C. Privacy Act In accordance with 5 U.S.C. 553(c), DOT solicits comments from the public to better inform its rulemaking process. DOT posts these comments, without edit, including any personal information the commenter provides, to www.regulations.gov, as described in the system of records notice (DOT/ALL-14 FDMS), which can be reviewed at www.transportation.gov/privacy. D. Advance Notice of Proposed Rulemaking (ANPRM) or Negotiated Rulemaking Not Required Under 49 U.S.C. 31136(g), added by section 5202 of the Fixing America's Surface Transportation or FAST Act, Public Law 114-94, 129 Stat. 1312, 1534 (Dec. 4, 2015), FMCSA is required either to proceed with negotiated rulemaking or to publish an ANPRM for any major rulemaking, unless the Agency finds good cause that an ANPRM is impracticable, unnecessary, or contrary to the public interest. FMCSA has determined that this interim final rule is not major; therefore, neither an ANPRM nor a negotiated rulemaking is required. II. Executive Summary A. Purpose and Summary of the Major Provisions This interim final rule delays the compliance date for several provisions in the Medical Examiner's Certification Integration final rule (80 FR 22790, Apr. 23, 2015) from June 22, 2018, to June 22, 2021. Specifically, it postpones, through June 22, 2021, the provisions for: (1) FMCSA to electronically, transmit from the National Registry to the SDLAs, driver identification information, examination results, and restriction information from examinations performed for holders of commercial learner's permits (CLPs) or commercial driver's licenses (CDLs) (interstate and intrastate); (2) FMCSA to electronically transmit to the SDLAs medical variance information for all commercial motor vehicle (CMV) drivers; (3) SDLAs to post on the Commercial Driver's License Information System (CDLIS) driver record the driver identification, examination results, and restriction information received electronically from FMCSA; and (4) motor carriers to no longer be required to verify that CLP/CDL drivers were certified by a certified medical examiner (ME) listed on the National Registry. B. Benefits and Costs This rule results in neither costs nor benefits but aligns the compliance dates with the date when the IT systems will be ready and, thus, when the costs and benefits estimated in the 2015 final rule can be realized. III. Legal Basis for the Interim Final Rule The legal basis of the 2015 final rule, set out at 80 FR 22791- 22792, also serves as the legal basis for this interim final rule. Brief summaries of the relevant legal bases for the actions taken in this interim final rule are set out below. A. Authority Over Drivers Affected Drivers Required To Obtain a Medical Examiners Certificate (MEC) FMCSA is required by statute to establish standards for the physical qualifications of drivers who operate CMVs in interstate commerce for non-excepted industries (49 U.S.C. 31136(a)(3) and 31502(b)). Subject to certain limited exceptions,\1\ FMCSA has fulfilled the statutory mandate by establishing physical qualification standards for all drivers covered by these provisions (49 CFR 391.11(b)(4)). Such drivers must obtain, from an ME, a certification indicating that the driver is physically qualified to drive a CMV (49 CFR 391.41(a), 391.43(g) and (h)). FMCSA is also required to ensure that the operation of a CMV does not have a deleterious effect on the physical condition of drivers (49 U.S.C. 31136(a)(4)). --------------------------------------------------------------------------- \1\ See 49 CFR 390.3(f) and 391.2. --------------------------------------------------------------------------- Drivers Required To Obtain a CDL The authority for FMCSA to require an operator of a CMV to obtain a CDL is based on 49 U.S.C. 31302 and the authority to set minimum standards for the testing and fitness of such operators rests on 49 U.S.C.31305. B. Authority To Regulate State CDL Programs Under 49 U.S.C. 31311 and 31314, FMCSA has authority to prescribe procedures and requirements the States must follow when issuing CDLs (see, generally, 49 CFR parts 383 and 384). In particular, under section 31314, in order to avoid loss of certain Federal-aid highway funds otherwise apportioned under 23 U.S.C. 104(b), each State must comply with the requirement in 49 U.S.C. 31311(a)(1) to adopt and carry out a program for testing and ensuring the fitness of individuals to operate CMVs consistent with the minimum standards prescribed by FMCSA under 49 U.S.C. 31305(a) (see also 49 CFR 384.201). C. Authority To Require Reporting by MEs FMCSA has authority under 49 U.S.C. 31133(a)(8) and 31149(c)(1)(E) to require MEs on the National Registry to obtain information from CMV drivers regarding their physical health, to record and retain the results of the physical examinations of CMV drivers, and to require frequent reporting of the information contained on the MECs they issue. Section 31133(a)(8) gives the Agency broad administrative powers (specifically ``to prescribe recordkeeping [[Page 28776]] and reporting requirements'') to assist in ensuring motor carrier safety and driver health (Sen. Report No. 98-424 at 9 (May 2, 1984)). Section 31149(c)(1)(E) authorizes a requirement for electronic reporting of certain specific information by MEs, including applicant names and numerical identifiers as determined by the FMCSA Administrator. Section 31149(c)(1)(E) sets minimum monthly reporting requirements for MEs and does not preclude the exercise by the Agency of its broad authority under section 31133(a)(8) to require more frequent and more inclusive reports.\2\ In addition to the general rulemaking authority in 49 U.S.C. 31136(a), the Secretary of Transportation is specifically authorized by section 31149(e) to ``issue such regulations as may be necessary to carry out this section.'' --------------------------------------------------------------------------- \2\ The provisions of section 31149(c)(1)(E) have been amended by section 32302(c)(1)(A) of Moving Ahead for Progress in the 21st Century, Public Law 112-141, 126 Stat. 405 (July 6, 2012) (``MAP- 21''). --------------------------------------------------------------------------- Authority to implement these various statutory provisions has been delegated to the Administrator of FMCSA (49 CFR 1.87(f)). IV. Background A. Regulatory History In 2008, FMCSA issued the Medical Certification Requirements as Part of the Commercial Driver's License (CDL) final rule (73 FR 73096, Dec. 1, 2008). This rule established requirements for CDL drivers to provide MEC information to SDLAs for posting on the driver record. Then the National Registry of Certified Medical Examiners final rule was issued to establish the National Registry and require that MEs listed on the National Registry perform all physical examinations of CMV drivers and issue MECs to them (77 FR 24104, Apr. 20, 2012). The provisions of these final rules are now in effect. The Medical Examiner's Certification Integration final rule adopted a number of changes in the procedures for the preparation, recording, and utilization of Medical Examination Report Forms and MECs for CMV drivers (80 FR 22790, Apr. 23, 2015; 80 FR 35577, Jun. 22, 2015). Some of those changes, such as the specific forms to be used by MEs to record the results of physical examinations and to certify CMV drivers as physically qualified, are already in effect.\3\ --------------------------------------------------------------------------- \3\ Judicial review of this aspect of the 2015 final rule was dismissed for lack of standing in Owner Operator Indep. Drivers Ass'n v. United States DOT, 878 F.3d 1099, 1102 (8th Cir. 2018) (rehearing and rehearing en banc) denied Apr. 2, 2018). --------------------------------------------------------------------------- But several provisions were adopted with a compliance date of June 22, 2018, a delay of 3 years, primarily to allow the SDLAs and FMCSA sufficient time to develop, test and install the necessary IT infrastructure to implement them. The final rule required MEs to report results of all CMV drivers' physical examinations performed (including the results of examinations where the driver was found not to be qualified) to FMCSA by midnight (local time) of the next calendar day following the examination. The reporting included results on all CMV drivers who are required to be medically certified to operate in interstate commerce, not only those who hold or apply for CLPs or CDLs. The reported results would be of any examinations performed in accordance with the Federal Motor Carrier Safety Regulations (FMCSRs), as well as those in accordance with any applicable State variances (which will be valid for intrastate operations only). For holders of CLPs/CDLs (interstate and intrastate), FMCSA stated that it would electronically transmit from the National Registry to the SDLAs the driver identification, examination results, and restriction information. The SDLAs would in turn be required to post this information to the CDLIS driver record. The Agency also said it would electronically transmit medical variance information for all CMV drivers to the SDLAs. If the information transmitted so required, the SDLAs were required to change the driver's certified status on the CDLIS driver record and/or begin a downgrade of the CLP/CDL. Motor carriers, enforcement personnel, and other interested parties would be permitted to rely on the medical certification information on the CDLIS driver record and would no longer be permitted to rely on the original paper MEC as proof of medical certification. The 2015 final rule also adopted new provisions based on the new reporting requirement for MEs that would invalidate any existing MEC held by a CMV driver whenever the driver failed a new physical qualification examination. If the driver involved was a CLP/CDL holder, such invalidation would be electronically transmitted from the National Registry to the SDLAs for the SDLA to change the certified status on the CDLIS driver record and/or begin a downgrade of the CLP/CDL. B. Recent Developments As the compliance date of June 22, 2018, draws nearer, FMCSA has reluctantly concluded that it will not be able to electronically transmit MEC information from the National Registry to the SDLAs by that date. Further, the SDLAs will not be able to electronically receive the MEC information from the National Registry for posting to the CDLIS driver record, as intended by the Medical Examiner's Certification Integration final rule. Although the Agency has initiated the IT development work to enhance the National Registry to enable the Agency to electronically transmit MEC information and medical variances to the States, along with the programming code the States would need to implement changes to their IT systems to receive the data, none of this work will be completed in time to meet the June 22, 2018 compliance date. Under these circumstances, neither the Agency nor the stakeholders would be able to rely on the CDLIS driver record as official proof of medical certification, unless drivers continue to provide the original paper MEC to the SDLAs, as is being done presently. All of the functions regarding electronic transmission of data that were to be implemented on June 22, 2018, are dependent upon the development and implementation of the IT infrastructure that will not be available on June 22, 2018. For this reason, FMCSA decided to extend the compliance date to June 22, 2021, to ensure that the SDLAs have sufficient time once the final specifications are released to make the necessary IT programming changes. V. Discussion of the Interim Final Rule This interim final rule is effective immediately and establishes, for most provisions in the 2015 final rule, a new compliance date of June 22, 2021. The specific provisions impacted by this change are listed in the Section-by-Section discussion below. This delayed compliance date means that through June 21, 2021: Certified MEs must continue issuing MECs to qualified CLP/ CDL applicants/holders; CLP/CDL applicants/holders must continue ensuring that the SDLA receives a copy of their MEC; Motor carriers must continue verifying that drivers were certified by an ME listed on the National Registry; and SDLAs must continue processing paper copies of MECs they receive from CLP/CDL applicants/holders. It should be noted that the compliance date in today's rule remains as June 22, 2018, for the requirement for MEs to report results of all CMV driver physical examinations performed (including the results of examinations where the driver was found not to be qualified) to FMCSA by midnight (local time) of the next calendar day following the examination. In other words, except for the ME reporting requirement, this [[Page 28777]] interim final rule continues the status quo for another 3 years. The details for these requirements can be found in the preambles of all three of the prior final rules, or in the current regulatory text in 49 CFR parts 383, 384 and 391. As noted above, FMCSA is not delaying the requirement for MEs performing physical examinations of CMV drivers to report results of all CMV drivers' physical examinations (including the results of examinations where the driver was found not to be qualified) to FMCSA by midnight (local time) of the next calendar day following the examination, since several MEs already submit such results more frequently than monthly. Having the MEs begin submitting reports by midnight (local time) of the next calendar day following the examination also allows FMCSA to begin electronically transmitting this important safety data to each State when that State is ready to receive the information, thereby providing States additional flexibility to implement the provisions of this rulemaking at their own pace. FMCSA believes some States may be prepared to receive this data ahead of the June 22, 2021, date to take advantage of the efficiencies and added security the new process affords. When FMCSA is ready to begin electronically transmitting MEC information from the National Registry, and an SDLA is ready to begin receiving this information electronically from the National Registry, FMCSA will work with the SDLA involved on the most appropriate means to use such electronic transmissions. FMCSA states that, under such circumstances, electronic transmission of the MEC information may be an acceptable means for CDL and CLP holders to satisfy the requirement of providing the MEC to the SDLA. In order to avoid any uncertainty, provisions are being added to the appropriate regulations stating that, in case of a conflict between the medical certification information provided electronically by FMCSA and information on a paper version of the MEC, the electronic record will be controlling. On the other hand, the provisions in the regulations governing the handling of these matters under the current procedures will remain in effect through June 21, 2021, to ensure continued compliance by SDLAs and other affected stakeholders until the electronic transmission of MEC information is operational for all SDLAs. If some SDLAs begin receiving MEC information from FMCSA prior to June 22, 2021, FMCSA and the SDLAs will make every effort to advise all stakeholders when such handling begins. MEs listed on the National Registry, employers and enforcement personnel (both State and Federal) will need to be made fully aware that some SDLAs may be following procedures different from the remaining States. VI. Good Cause Exists Although the promulgation of a final rule adjusting compliance dates would ordinarily involve the issuance of a notice of proposed rulemaking (NPRM) and an opportunity for public comment, the Administrative Procedure Act does permit their omission for good cause, when ``notice and public procedure thereon are impracticable, unnecessary, or contrary to the public interest'' (5 U.S.C. 553(b)(B)). The necessary IT infrastructure to enable stakeholders to comply with the regulatory provisions involved will not be available on June 22, 2018. Under these circumstances, and in order to timely clarify the applicable regulatory requirements, FMCSA finds that there is good cause to issue this interim final rule. A proposed rule allowing prior notice and opportunity for comment could not be completed before June 22 and is therefore both impractical and contrary to the public interest. An opportunity for public comment is provided after publication of the interim final rule. All comments will be reviewed and the interim final rule may be amended as a result of those comments. In addition, upon a finding of good cause, the Agency may provide for a final rule to become effective less than 30 days after publication in the Federal Register (5 U.S.C. 553(d)(3)). Therefore, for the same reasons as indicated above, the Agency makes this interim final rule effective immediately upon publication in the Federal Register. VII. International Impacts The FMCSRs, and any exceptions to the FMCSRs, apply only within the United States (and, in some cases, United States territories). Motor carriers and drivers are subject to the laws and regulations of the countries in which they operate, unless an international agreement states otherwise. Drivers and carriers should be aware of the regulatory differences among nations. VIII. Section-by-Section Analysis A. Parts 383, 384, and 391 In parts 383, 384, and 391, FMCSA makes a few clarifying edits and changes the date of the rule as stated in the table below. Table 1--Date Changes ------------------------------------------------------------------------ Existing language in the CFR that Language added to the Section that is changed: is removed today: CFR by today's final rule: ------------------------------------------------------------------------ 383.71(h)(1)(i)............... June 22, 2018.... June 22, 2021. 383.71(h)(1)(ii).............. June 22, 2018.... June 22, 2021. 383.71(h)(3)(i)............... June 22, 2018.... June 22, 2021. 383.71(h)(3)(ii).............. June 22, 2018.... June 22, 2021. 383.73(a)(2)(vii)(A).......... June 22, 2018.... June 22, 2021. 383.73(a)(2)(vii)(B).......... June 22, 2018.... June 22, 2021. 383.73(b)(5)(i)............... June 22, 2018.... June 22, 2021. 383.73(b)(5)(ii).............. June 22, 2018.... June 22, 2021. 383.73(o)(1)(i)............... June 22, 2018.... June 22, 2021. 383.73(o)(1)(ii).............. June 22, 2018.... June 22, 2021. 383.73(o)(2)(i)............... June 22, 2018.... June 22, 2021. 383.73(o)(2)(ii).............. June 22, 2018.... June 22, 2021. 383.73(o)(3)(i)............... June 22, 2018.... June 22, 2021. 383.73(o)(3)(ii).............. June 22, 2018.... June 22, 2021. 383.73(o)(4)(i)(A)(1)......... June 22, 2018.... June 22, 2021. 383.73(o)(4)(i)(A)(2)......... June 22, 2018.... June 22, 2021. 383.73(o)(4)(ii)(A)........... June 22, 2018.... June 22, 2021. 383.73(o)(4)(ii)(B)........... June 22, 2018.... June 22, 2021. [[Page 28778]] 384.301(i).................... June 22, 2018.... June 22, 2021. 391.23(m)(2)(i)(B)(1)......... June 22, 2018.... June 21, 2021. 391.23(m)(2)(i)(C)............ June 22, 2018.... June 21, 2021. 391.23(m)(3)(i)(B)(1)......... June 22, 2018.... June 21, 2021. 391.23(m)(3)(i)(C)............ June 22, 2018.... June 21, 2021. 391.41(a)(2)(i)(A)............ June 22, 2018.... June 21, 2021. 391.41(a)(2)(i)(B)............ June 22, 2018.... June 22, 2021. 391.43(g)(2)(i)............... June 22, 2018.... June 22, 2021. 391.43(g)(2)(ii).............. June 22, 2018.... June 22, 2021. 391.43(g)(3).................. June 22, 2018.... June 22, 2021. 391.45(d)..................... June 22, 2018.... June 22, 2021. 391.51(b)(7)(ii).............. June 22, 2018.... June 21, 2021. 391.51(b)(9)(ii).............. June 22, 2018.... June 21, 2021. ------------------------------------------------------------------------ B. Sections 383.71(h)(4), 383.73(o)(6) and 391.23(m)(4) Identical new paragraphs are added to Sec. Sec. 383.71(h)(4), 383.73(o)(6), and 391.23(m)(4). The added text states that in the event of a conflict between the medical certification information provided electronically by FMCSA and a paper copy of the MEC, the medical certification information provided electronically by FMCSA shall control. C. Section 391.41 In addition to the changes in the compliance dates in Sec. 391.41 noted in the table above, FMCSA adds the phrase ``and through June 21, 2021'' to Sec. 391.41(a)(2)(ii), following the phrase, ``Beginning on July 8, 2015.'' This provides an ending date for the provision that CLP holders, while operating a CMV, would be required to carry their MEC, or a copy, for up to 15 days after the date they were issued. FMCSA also adds a new paragraph (a)(2)(iv) that states that in the event of a conflict between the medical certification information provided electronically by FMCSA and a paper copy of the MEC, the medical certification information provided electronically by FMCSA shall control. IX. Regulatory Analyses A. Executive Order (E.O.) 12866 (Regulatory Planning and Review), E.O. 13563 (Improving Regulation and Regulatory Review), and DOT Regulatory Policies and Procedures FMCSA has determined that this interim final rule is not a significant regulatory action under section 3(f) of E.O. 12866 (58 FR 51735, Oct. 4, 1993), Regulatory Planning and Review, as supplemented by E.O. 13563 (76 FR 3821, Jan. 21, 2011), Improving Regulation and Regulatory Review, and does not require an assessment of potential costs and benefits under section 6(a)(3) of that Order. Accordingly, the Office of Management and Budget (OMB) has not reviewed it under that Order. It is also not significant within the meaning of DOT regulatory policies and procedures (DOT Order 2100.5 dated May 22, 1980 (44 FR 11034, Feb. 26, 1979). The Medical Examiner's Certification Integration Final Rule, published April 23, 2015 (80 FR 22790), amended the FMCSRs to establish a streamlined process for SDLAs to receive CMV driver physical examination results from the MEs, via the National Registry. The 2015 final rule estimated that the National Registry would be able to receive and transmit this information on a daily basis by June 22, 2018, and established compliance dates for MEs, motor carriers, FMCSA, and the States accordingly. This rule, effective today, delays until June 22, 2021, the compliance date requiring (1) FMCSA to electronically transmit from the National Registry to the SDLAs driver identification information, examination results, and restriction information from examinations performed for holders of CLPs/CDLs (interstate and intrastate); (2) FMCSA to electronically transmit to the SDLAs medical variance information for all CMV drivers; (3) SDLAs to post driver identification, examination results, and restriction information received electronically from FMCSA; and (4) motor carriers will no longer need to verify that their drivers holding CLPs or CDLs were certified by an ME listed on the National Registry. This action is being taken to ensure that SDLAs have sufficient time to make the necessary IT programming changes. Although this rule impacts the responsibilities of MEs, CMV drivers, motor carriers, SDLAs, and FMCSA, it is not expected to generate any economic costs or benefits. The 2015 final rule accounted for costs associated with system development and implementation, and benefits associated with streamlined processes and reduced paperwork. These costs and benefits (originally anticipated to be realized on the June 22, 2018, compliance date) will not be realized on June 22, 2018. Therefore, the baseline against which to evaluate the impacts of this interim final rule is that the necessary systems will not be ready on June 22, 2018, and will instead be ready on June 22, 2021. This rule aligns the compliance date with the date when the systems will be ready and thus, when the costs and benefits estimated in the 2015 final rule can be realized. This rule does not result in additional costs or benefits, nor does it inhibit the realization of the costs and benefits identified in the 2015 final rule. B. E.O. 13771 (Reducing Regulation and Controlling Regulatory Costs) This interim final rule is not an E.O. 13771 regulatory action because this rule is not significant under E.O. 12866.\4\ --------------------------------------------------------------------------- \4\ Executive Office of the President, Office of Management and Budget. Guidance Implementing Executive Order 13771, Titled ``Reducing Regulation and Controlling Regulatory Costs.'' Memorandum M-17-21. April 5, 2017. --------------------------------------------------------------------------- C. Regulatory Flexibility Act (Small Entities) Under the Regulatory Flexibility Act of 1980 (5 U.S.C. 601-612), FMCSA is not required to complete a regulatory flexibility analysis, because, as discussed earlier in the Good Cause Exists section, this action is not subject to notice and comment under section [[Page 28779]] 553(b) of the Administrative Procedure Act.\5\ --------------------------------------------------------------------------- \5\ 5 U.S.C 553(b). --------------------------------------------------------------------------- Act. D. Assistance for Small Entities In accordance with section 213(a) of the Small Business Regulatory Enforcement Fairness Act of 1996, FMCSA wants to assist small entities in understanding this interim final rule so that they can better evaluate its effects on themselves and participate in the rulemaking initiative. If the interim final rule will affect your small business, organization, or governmental jurisdiction and you have questions concerning its provisions or options for compliance; please consult the FMCSA point of contact, Ms. Christine A. Hydock listed in the For Further Information Contact section of this interim final rule. Small businesses may send comments on the actions of Federal employees who enforce or otherwise determine compliance with Federal regulations to the Small Business Administration's Small Business and Agriculture Regulatory Enforcement Ombudsman and the Regional Small Business Regulatory Fairness Boards. The Ombudsman evaluates these actions annually and rates each agency's responsiveness to small business. If you wish to comment on actions by employees of FMCSA, call 1-888-REG-FAIR (1-888-734-3247). DOT has a policy regarding the rights of small entities to regulatory enforcement fairness and an explicit policy against retaliation for exercising these rights. E. Unfunded Mandates Reform Act of 1995 The Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1531-1538) requires Federal agencies to assess the effects of their discretionary regulatory actions. The Act addresses actions that may result in the expenditure by a State, local, or tribal government, in the aggregate, or by the private sector of $156 million (which is the value equivalent of $100 million in 1995, adjusted for inflation to 2015 levels) or more in any one year. Though this interim final rule will not result in such an expenditure, the Agency does discuss the effects of this rule elsewhere in this preamble. F. Paperwork Reduction Act This interim final rule calls for no new collection of information under the Paperwork Reduction Act of 1995 (44 U.S.C. 3501-3520). G. E.O. 13132 (Federalism) A rule has implications for Federalism under section 1(a) of Executive Order 13132 if it has ``substantial direct effects on the States, on the relationship between the national government and the States, or on the distribution of power and responsibilities among the various levels of government.'' FMCSA has determined that this interim final rule would not have substantial direct costs on or for States, nor would it limit the policymaking discretion of States. Nothing in this document preempts any State law or regulation. Therefore, this rule does not have sufficient federalism implications to warrant the preparation of a Federalism Impact Statement. H. E.O. 12988 (Civil Justice Reform) This interim final rule meets applicable standards in sections 3(a) and 3(b)(2) of E.O. 12988, Civil Justice Reform, to minimize litigation, eliminates ambiguity, and reduce burden. I. E.O. 13045 (Protection of Children) E.O. 13045, Protection of Children from Environmental Health Risks and Safety Risks (62 FR 19885, Apr. 23, 1997), requires agencies issuing ``economically significant'' rules, if the regulation also concerns an environmental health or safety risk that an agency has reason to believe may disproportionately affect children, to include an evaluation of the regulation's environmental health and safety effects on children. The Agency determined this interim final rule is not economically significant. Therefore, no analysis of the impacts on children is required. In any event, the Agency does not anticipate that this regulatory action could in any respect present an environmental or safety risk that could disproportionately affect children. J. E.O. 12630 (Taking of Private Property) FMCSA reviewed this interim final rule in accordance with E.O. 12630, Governmental Actions and Interference with Constitutionally Protected Property Rights, and has determined it will not effect a taking of private property or otherwise have taking implications. K. Privacy Section 522 of title I of division H of the Consolidated Appropriations Act, 2005, enacted December 8, 2004 (Pub. L. 108-447, 118 Stat. 2809, 3268, 5 U.S.C. 552a note), requires the Agency to conduct a privacy impact assessment (PIA) of a regulation that will affect the privacy of individuals. This rule does not require the collection of personally identifiable information (PII). The supporting PIA, available for review in the docket, gives a full and complete explanation of FMCSA practices for protecting PII in general and specifically in relation to this interim final rule. The Privacy Act (5 U.S.C. 552a) applies only to Federal agencies and any non-Federal agency which receives records contained in a system of records from a Federal agency for use in a matching program. The E-Government Act of 2002, Public Law 107-347, section 208, 116 Stat. 2899, 2921 (Dec. 17, 2002), requires Federal agencies to conduct a PIA for new or substantially changed technology that collects, maintains, or disseminates information in an identifiable form. No new or substantially changed technology would collect, maintain, or disseminate information because of this rule. As a result, FMCSA has not conducted a privacy impact assessment. L. E.O. 12372 (Intergovernmental Review) The regulations implementing E.O. 12372 regarding intergovernmental consultation on Federal programs and activities do not apply to this program. M. E.O. 13211 (Energy Supply, Distribution, or Use) FMCSA has analyzed this interim final rule under E.O. 13211, Actions Concerning Regulations That Significantly Affect Energy Supply, Distribution, or Use. The Agency has determined that it is not a ``significant energy action'' under that order because it is not a ``significant regulatory action'' likely to have a significant adverse effect on the supply, distribution, or use of energy. Therefore, it does not require a Statement of Energy Effects under E.O. 13211. The Administrator of the Office of Information and Regulatory Affairs has not designated it as a significant energy action. Therefore, it does not require a Statement of Energy Effects under E.O. 13211. N. E.O. 13783 (Promoting Energy Independence and Economic Growth) E.O. 13783 directs executive departments and agencies to review existing regulations that potentially burden the development or use of domestically produced energy resources, and to appropriately suspend, revise, or rescind those that unduly burden the development of domestic energy resources. In accordance with E.O. 13783, DOT prepared and submitted a report to the Director of OMB that provides specific [[Page 28780]] recommendations that, to the extent permitted by law, could alleviate or eliminate aspects of agency action that burden domestic energy production. This interim final rule has not been identified by DOT under E.O. 13783 as potentially alleviating unnecessary burdens on domestic energy production. O. E.O. 13175 (Indian Tribal Governments) This interim final rule does not have tribal implications under E.O. 13175, Consultation and Coordination with Indian Tribal Governments, because it does not have a substantial direct effect on one or more Indian tribes, on the relationship between the Federal Government and Indian tribes, or on the distribution of power and responsibilities between the Federal Government and Indian tribes. P. National Technology Transfer and Advancement Act (Technical Standards) The National Technology Transfer and Advancement Act (NTTAA) (15 U.S.C. 272 note) directs agencies to use voluntary consensus standards in their regulatory activities unless the agency provides Congress, through OMB, with an explanation of why using these standards would be inconsistent with applicable law or otherwise impractical. Voluntary consensus standards (e.g., specifications of materials, performance, design, or operation; test methods; sampling procedures; and related management systems practices) are standards that are developed or adopted by voluntary consensus standards bodies. This interim final rule does not use technical standards. Therefore, FMCSA did not consider the use of voluntary consensus standards. Q. Environment (NEPA, CAA, Environmental Justice) FMCSA analyzed this interim final rule for the purpose of the National Environmental Policy Act of 1969 (42 U.S.C. 4321 et seq.), and determined this action is categorically excluded from further analysis and documentation in an environmental assessment or environmental impact statement under FMCSA Order 5610.1(69 FR 9680, Mar. 1, 2004), Appendix 2, paragraph (s)(7) and paragraph (t)(2). The Categorical Exclusion (CE) in paragraph (s)(7) covers requirements for State-issued commercial license documentation and paragraph (t)(2) addresses regulations that assure States have the appropriate information systems and procedures concerning CDL qualifications. The content in this interim final rule is covered by these CEs and the final action does not have any effect on the quality of the environment. The CE determination is available for inspection or copying in the Regulations.gov website listed under ADDRESSES. FMCSA also analyzed this rule under section 176(c) of the Clean Air Act, as amended (CAA) (42 U.S.C. 7401 et seq.), and implementing regulations promulgated by the Environmental Protection Agency. Approval of this action is exempt from the CAA's general conformity requirement since it does not affect direct or indirect emissions of criteria pollutants. Under E.O. 12898, each Federal agency must identify and address, as appropriate, ``disproportionately high and adverse human health or environmental effects of its programs, policies, and activities on minority populations and low-income populations'' in the United States, its possessions, and territories. FMCSA evaluated the environmental justice effects of this interim final rule in accordance with the E.O., and has determined that no environmental justice issue is associated with this interim final rule, nor is there any collective environmental impact that would result from its promulgation. List of Subjects 49 CFR Part 383 Administrative practice and procedure, Alcohol abuse, Drug abuse, Highway safety, Motor carriers. 49 CFR Part 384 Administrative practice and procedure, Alcohol abuse, Drug abuse, Highway safety, Motor carriers. 49 CFR Part 391 Alcohol abuse, Drug abuse, Drug testing, Highway safety, Motor carriers, Reporting and recordkeeping requirements, Safety, Transportation. In consideration of the foregoing, FMCSA amends 49 CFR chapter III, parts 383, 384, and 391 to read as follows: PART 383--COMMERCIAL DRIVER'S LICENSE STANDARDS; REQUIREMENTS AND PENALTIES 0 1. The authority citation for part 383 continues to read as follows: Authority: 49 U.S.C. 521, 31136, 31301 et seq., and 31502; secs. 214 and 215 of Pub. L. 106-159, 113 Stat. 1748, 1766, 1767; sec. 1012(b) of Pub. L. 107-56, 115 Stat. 272, 297, sec. 4140 of Pub. L. 109-59, 119 Stat. 1144, 1746; sec. 32934 of Pub. L. 112-141, 126 stat. 405, 830; and 49 CFR 1.87. 0 2. Amend Sec. 383.71 by revising paragraphs (h)(1) and (3), and adding paragraph (h)(4), to read as follows: Sec. 383.71 Driver application and certification procedures. * * * * * (h) * * * (1) New CLP and CDL applicants. (i) Before June 22, 2021, a new CLP or CDL applicant who certifies that he/she will operate CMVs in non- excepted, interstate commerce must provide the State with an original or copy (as required by the State) of a medical examiner's certificate prepared by a medical examiner, as defined in 49 CFR 390.5, and the State will post a medical qualifications status of ``certified'' on the CDLIS driver record for the driver; (ii) On or after June 22, 2021, a new CLP or CDL applicant who certifies that he/she will operate CMVs in non-excepted, interstate commerce must be medically examined and certified in accordance with 49 CFR 391.43 as medically qualified to operate a CMV by a medical examiner, as defined in 49 CFR 390.5. Upon receiving an electronic copy of the medical examiner's certificate from FMCSA, the State will post a medical qualifications status of ``certified'' on the CDLIS driver record for the driver; * * * * * (3) Maintaining the medical certification status of ``certified.'' (i) Before June 22, 2021, in order to maintain a medical certification status of ``certified,'' a CLP or CDL holder who certifies that he/she will operate CMVs in non-excepted, interstate commerce must provide the State with an original or copy (as required by the State) of each subsequently issued medical examiner's certificate; (ii) On or after June 22, 2021, in order to maintain a medical certification status of ``certified,'' a CLP or CDL holder who certifies that he/she will operate CMVs in non-excepted, interstate commerce must continue to be medically examined and certified in accordance with 49 CFR 391.43 as physically qualified to operate a commercial motor vehicle by a medical examiner, as defined in 49 CFR 390.5. FMCSA will provide the State with an electronic copy of the medical examiner's certificate information for all subsequent medical examinations in which the driver has been deemed qualified. (4) In the event of a conflict between the medical certification information provided electronically by FMCSA and a paper copy of the medical examiner's certificate, the medical certification [[Page 28781]] information provided electronically by FMCSA shall control. 0 3. Amend Sec. 383.73 by revising paragraphs (a)(2)(vii), (b)(5), (o)(1)(i) introductory text, (o)(1)(ii) introductory text, (o)(2), (o)(3), (o)(4)(i)(A), and (o)(4)(ii), and adding paragraph (o)(6), to read as follows: Sec. 383.73 State procedures (a) * * * (2) * * * (vii)(A) Before June 22, 2021, for drivers who certified their type of driving according to Sec. 383.71(b)(1)(i) (non-excepted interstate) and, if the CLP applicant submits a current medical examiner's certificate, date-stamp the medical examiner's certificate, and post all required information from the medical examiner's certificate to the CDLIS driver record in accordance with paragraph (o) of this section. (B) On or after June 22, 2021, for drivers who certified their type of driving according to Sec. 383.71(b)(1)(i) (non-excepted interstate) and, if FMCSA provides current medical examiner's certificate information electronically, post all required information matching the medical examiner's certificate to the CDLIS driver record in accordance with paragraph (o) of this section. (b) * * * (5)(i) Before June 22, 2021, for drivers who certified their type of driving according to Sec. 383.71(b)(1)(i) (non-excepted interstate) and, if the CDL holder submits a current medical examiner's certificate, date-stamp the medical examiner's certificate and post all required information from the medical examiner's certificate to the CDLIS driver record in accordance with paragraph (o) of this section. (ii) On or after June 22, 2021, for drivers who certified their type of driving according to Sec. 383.71(b)(1)(i) (non-excepted interstate) and, if FMCSA provides current medical examiner's certificate information electronically, post all required information matching the medical examiner's certificate to the CDLIS driver record in accordance with paragraph (o) of this section. * * * * * (o) * * * (1)(i) Status of CLP or CDL holder. Before June 22, 2021, for each operator of a commercial motor vehicle required to have a CLP or CDL, the current licensing State must: * * * * * (ii) Status of CLP or CDL holder. On or after June 22, 2021, for each operator of a commercial motor vehicle required to have a CLP or CDL, the current licensing State must: * * * * * (2) Status update. (i) Before June 22, 2021, the State must, within 10 calendar days of the driver's medical examiner's certificate or medical variance expiring, the medical variance being rescinded or the medical examiner's certificate being voided by FMCSA, update the medical certification status of that driver as ``not certified.'' (ii) On or after June 22, 2021, the State must, within 10 calendar days of the driver's medical examiner's certificate or medical variance expiring, the medical examiner's certificate becoming invalid, the medical variance being rescinded or the medical examiner's certificate being voided by FMCSA, update the medical certification status of that driver as ``not certified.'' (3) Variance update. (i) Before June 22, 2021, within 10 calendar days of receiving information from FMCSA regarding issuance or renewal of a medical variance for a driver, the State must update the CDLIS driver record to include the medical variance information provided by FMCSA. (ii) On or after June 22, 2021, within 1 business day of electronically receiving medical variance information from FMCSA regarding the issuance or renewal of a medical variance for a driver, the State must update the CDLIS driver record to include the medical variance information provided by FMCSA. (4) * * * (i) * * * (A)(1) Before June 22, 2021, notify the CLP or CDL holder of his/ her CLP or CDL ``not-certified'' medical certification status and that the CMV privileges will be removed from the CLP or CDL unless the driver submits a current medical examiner's certificate and/or medical variance, or changes his/her self-certification to driving only in excepted or intrastate commerce (if permitted by the State); (2) On or after June 22, 2021, notify the CLP or CDL holder of his/ her CLP or CDL ``not-certified'' medical certification status and that the CMV privileges will be removed from the CLP or CDL unless the driver has been medically examined and certified in accordance with 49 CFR 391.43 as physically qualified to operate a commercial motor vehicle by a medical examiner, as defined in 49 CFR 390.5, or the driver changes his/her self-certification to driving only in excepted or intrastate commerce (if permitted by the State). * * * * * (ii)(A) Before June 22, 2021, if a driver fails to provide the State with the certification contained in Sec. 383.71(b)(1), or a current medical examiner's certificate if the driver self-certifies according to Sec. 383.71(b)(1)(i) that he/she is operating in non- excepted interstate commerce as required by Sec. 383.71(h), the State must mark that CDLIS driver record as ``not-certified'' and initiate a CLP or CDL downgrade following State procedures in accordance with paragraph (o)(4)(i)(B) of this section. (B) On or after June 22, 2021, if a driver fails to provide the State with the certification contained in Sec. 383.71(b)(1), or, if the driver self-certifies according to Sec. 383.71(b)(1)(i) that he/ she is operating in non-excepted interstate commerce as required by Sec. 383.71(h) and the information required by paragraph (o)(2)(ii) of this section is not received and posted, the State must mark that CDLIS driver record as ``not-certified'' and initiate a CLP or CDL downgrade following State procedures in accordance with paragraph (o)(4)(i)(B) of this section. * * * * * (6) In the event of a conflict between the medical certification information provided electronically by FMCSA and a paper copy of the medical examiner's certificate, the medical certification information provided electronically by FMCSA shall control. * * * * * PART 384--STATE COMPLIANCE WITH COMMERCIAL DRIVER'S LICENSE PROGRAM 0 4. The authority citation for part 384 continues to read as follows: Authority: 49 U.S.C. 31136, 31301, et seq., and 31502; secs. 103 and 215 of Pub. L. 106-59, 113 Stat. 1753, 1767; sec. 32934 of Pub. L. 112-141, 126 stat. 405, 830 and 49 CFR 1.87. 0 5. Amend Sec. 384.301 by revising paragraph (i) to read as follows: Sec. 384.301 Substantial compliance-general requirements. * * * * * (i) A State must come into substantial compliance with the requirements of subpart B of this part and part 383 of this chapter in effect as of June 22, 2015, as soon as practical, but, unless otherwise specifically provided in this part, not later than June 22, 2021. * * * * * PART 391--QUALIFICATIONS OF DRIVERS AND LONGER COMBINATION VEHICLE (LCV) DRIVER INSTRUCTORS 0 6. The authority citation for part 391 continues to read as follows: [[Page 28782]] Authority: 49 U.S.C. 504, 508, 31133, 31136, 31149, and 31502; sec. 4007(b) of Pub. L. 102-240, 105 Stat. 1914, 2152; sec. 114 of Pub. L. 103-311, 108 Stat. 1673, 1677; sec. 215 of Pub. L. 106-159, 113 Stat. 1748, 1767; sec. 32934 of Pub. L. 112-141, 126 Stat. 405, 830; sec. 5524 of Pub. L. 114-94, 129 Stat. 1312, 1560; and 49 CFR 1.87. 0 7. Amend Sec. 391.23 by revising paragraphs (m)(2)(i)(B)(1) and (m)(2)(i)(C), (m)(3)(i)(B)(1) and (m)(3)(i)(C), and adding paragraph (m)(4), to read as follows: Sec. 391.23 Investigation and inquiries. * * * * * (m) * * * (2) * * * (i) * * * (B)(1) Beginning on May 21, 2014, and through June 21, 2021, that the driver was certified by a medical examiner listed on the National Registry of Certified Medical Examiners as of the date of medical examiner's certificate issuance. * * * * * (C) Exception. Beginning on January 30, 2015, and through June 21, 2021, if the driver provided the motor carrier with a copy of the current medical examiner's certificate that was submitted to the State in accordance with Sec. 383.73(b)(5) of this chapter, the motor carrier may use a copy of that medical examiner's certificate as proof of the driver's medical certification for up to 15 days after the date it was issued. * * * * * (3) * * * (i) * * * (B)(1) Through June 21, 2021, that the driver was certified by a medical examiner listed on the National Registry of Certified Medical Examiners as of the date of medical examiner's certificate issuance. * * * * * (C) Through June 21, 2021, if the driver provided the motor carrier with a copy of the current medical examiner's certificate that was submitted to the State in accordance with Sec. 383.73(a)(2)(vii) of this chapter, the motor carrier may use a copy of that medical examiner's certificate as proof of the driver's medical certification for up to 15 days after the date it was issued. * * * * * (4) In the event of a conflict between the medical certification information provided electronically by FMCSA and a paper copy of the medical examiner's certificate, the medical certification information provided electronically by FMCSA shall control. 0 8. Amend Sec. 391.41 by revising paragraphs (a)(2)(i) and (ii), and adding paragraph (a)(2)(iv), to read as follows: Sec. 391.41 Physical qualifications for drivers. (a) * * * (2) * * * (i)(A) Beginning on January 30, 2015 and through June 21, 2021, a driver required to have a commercial driver's license under part 383 of this chapter, and who submitted a current medical examiner's certificate to the State in accordance with 49 CFR 383.71(h) documenting that he or she meets the physical qualification requirements of this part, no longer needs to carry on his or her person the medical examiner's certificate specified at Sec. 391.43(h), or a copy, for more than 15 days after the date it was issued as valid proof of medical certification. (B) On or after June 22, 2021, a driver required to have a commercial driver's license or a commercial learner's permit under 49 CFR part 383, and who has a current medical examiner's certificate documenting that he or she meets the physical qualification requirements of this part, no longer needs to carry on his or her person the medical examiner's certificate specified at Sec. 391.43(h). (ii) Beginning on July 8, 2015, and through June 21, 2021, a driver required to have a commercial learner's permit under part 383 of this chapter, and who submitted a current medical examiner's certificate to the State in accordance with Sec. 383.71(h) of this chapter documenting that he or she meets the physical qualification requirements of this part, no longer needs to carry on his or her person the medical examiner's certificate specified at Sec. 391.43(h), or a copy for more than 15 days after the date it was issued as valid proof of medical certification. * * * * * (iv) In the event of a conflict between the medical certification information provided electronically by FMCSA and a paper copy of the medical examiner's certificate, the medical certification information provided electronically by FMCSA shall control. * * * * * 0 9. Amend Sec. 391.43 by revising paragraphs (g)(2) and (3) to read as follows: Sec. 391.43 Medical examination; certificate of physical examination. * * * * * (g) * * * (2)(i) Before June 22, 2021, if the medical examiner finds that the person examined is physically qualified to operate a commercial motor vehicle in accordance with Sec. 391.41(b), he or she must complete a certificate in the form prescribed in paragraph (h) of this section and furnish the original to the person who was examined. The examiner must provide a copy to a prospective or current employing motor carrier who requests it. (ii) On or after June 22, 2021, if the medical examiner identifies that the person examined will not be operating a commercial motor vehicle that requires a commercial driver's license or a commercial learner's permit and finds that the driver is physically qualified to operate a commercial motor vehicle in accordance with Sec. 391.41(b), he or she must complete a certificate in the form prescribed in paragraph (h) of this section and furnish the original to the person who was examined. The examiner must provide a copy to a prospective or current employing motor carrier who requests it. (3) On or after June 22, 2021, if the medical examiner finds that the person examined is not physically qualified to operate a commercial motor vehicle in accordance with Sec. 391.41(b), he or she must inform the person examined that he or she is not physically qualified, and that this information will be reported to FMCSA. All medical examiner's certificates previously issued to the person are not valid and no longer satisfy the requirements of Sec. 391.41(a). * * * * * 0 10. Amend Sec. 391.45 by revising paragraph (d) to read as follows: Sec. 391.45 Persons who must be medically examined and certified. * * * * * (d) On or after June 22, 2021, any person found by a medical examiner not to be physically qualified to operate a commercial motor vehicle under the provisions of paragraph (g)(3) of Sec. 391.43. 0 11. Amend Sec. 391.51 by revising paragraphs (b)(7)(ii) and (b)(9)(ii) to read as follows: Sec. 391.51 General requirements for driver qualification files. * * * * * (b) * * * (7) * * * (ii) Exception. For CDL holders, beginning January 30, 2012, if the CDLIS motor vehicle record contains medical certification status information, the motor carrier employer must meet this requirement by obtaining the CDLIS motor vehicle record defined at Sec. 384.105 of this chapter. That record must be obtained from the current licensing State and placed in the driver qualification file. After January 30, [[Page 28783]] 2015, a non-excepted, interstate CDL holder without medical certification status information on the CDLIS motor vehicle record is designated ``not-certified'' to operate a CMV in interstate commerce. After January 30, 2015 and through June 21, 2021, a motor carrier may use a copy of the driver's current medical examiner's certificate that was submitted to the State for up to 15 days from the date it was issued as proof of medical certification. * * * * * (9) * * * (ii) Through June 21, 2021, for drivers required to have a CDL, a note relating to verification of medical examiner listing on the National Registry of Certified Medical Examiners required by Sec. 391.23(m)(2). * * * * * Issued under authority delegated in 49 CFR 1.87 on: June 15, 2018. Raymond P. Martinez, Administrator. [FR Doc. 2018-13314 Filed 6-20-18; 8:45 am] BILLING CODE 4910-EX-P
![28774 Federal Register / Vol. 83, No. 120 / Thursday, June 21, 2018 / Rules and Regulations
human health or environmental effects Authority: 5 U.S.C. 301 and 41 U.S.C. 140, 1200 New Jersey Avenue SE,
on minority or low-income populations 418b. Washington, DC, between 9 a.m. and 5
because it does not affect the level of 1552.219–70 [Removed and reserved]
p.m., Monday through Friday, except
protection provided to human health or Federal holidays.
the environment. This rulemaking does ■ 4. Section 1552.219–70 is removed • Fax: 202–493–2251.
not involve human health or and reserved. To avoid duplication, please use only
environmental effects. 1552.219–71 [Removed and reserved] one of these four methods. See the
‘‘Public Participation and Request for
K. Congressional Review ■ 5. Section 1552.219–71 is removed Comments’’ portion of the
and reserved. SUPPLEMENTARY INFORMATION section for
The Congressional Review Act, 5
[FR Doc. 2018–13349 Filed 6–20–18; 8:45 am] instructions on submitting comments,
U.S.C. 801 et seq., as added by the Small
Business Regulatory Enforcement BILLING CODE 6560–50–P including collection of information
Fairness Act of 1996, generally provides comments for the Office of Information
that before a rule may take effect, the and Regulatory Affairs, OMB.
agency promulgating the rule must DEPARTMENT OF TRANSPORTATION FOR FURTHER INFORMATION CONTACT: Ms.
submit a rule report, which includes a Christine A. Hydock, Chief, Medical
copy of the rule, to each House of the Federal Motor Carrier Safety Programs Division, Federal Motor
Congress and to the Comptroller General Administration Carrier Safety Administration, 1200
of the United States. Section 804 New Jersey Avenue SE, Washington, DC
exempts from section 801 the following 49 CFR Parts 383, 384, and 391 20590–0001, by telephone at 202–366–
types of rules (1) rules of particular [Docket No. FMCSA–2018–0152] 4001, or by email at fmcsamedical@
applicability; (2) rules relating to agency dot.gov. If you have questions on
RIN 2126–AC18
management or personnel; and (3) rules viewing or submitting material to the
of agency organization, procedure, or Extension of Compliance Dates for docket, contact Docket Services,
practice that do not substantially affect Medical Examiner’s Certification telephone (202) 366–9826.
the rights or obligations of non-agency Integration SUPPLEMENTARY INFORMATION:
parties. 5 U.S.C. 804(3). EPA is not
required to submit a rule report AGENCY: Federal Motor Carrier Safety I. Rulemaking Documents
regarding this action under section 801 Administration (FMCSA), DOT. A. Submitting Comments
because this is a rule of agency ACTION: Interim final rule; request for If you submit a comment, please
organization, procedure, or practice that comments. include the docket number for this
does not substantially affect the rights or interim final rule (Docket No. FMCSA–
obligations of non-agency parties. EPA SUMMARY: FMCSA amends its
regulations to delay the compliance date 2018–0152), indicate the specific
will use SBA’s federal wide mentor section of this document to which each
protégé program instead of managing its from June 22, 2018, to June 22, 2021, for
several provisions of its April 23, 2015 comment applies, and provide a reason
own program. for each suggestion or recommendation.
Medical Examiner’s Certification
List of Subjects in 48 CFR Parts 1519 Integration final rule. This action is You may submit your comments and
and 1552 being taken to provide FMCSA material online or by fax, mail, or hand
additional time to complete certain delivery, but please use only one of
Environmental protection,
information technology (IT) system these means. FMCSA recommends that
Government procurement, Reporting
development tasks for its National you include your name and a mailing
and recordkeeping requirements, Small
Registry of Certified Medical Examiners address, an email address, or a phone
businesses.
(National Registry) and provide the number in the body of your document
Dated: May 16, 2018. so that FMCSA can contact you if there
State Driver’s Licensing Agencies
Kimberly Patrick,
(SDLAs) sufficient time to make the are questions regarding your
Director, Office of Acquisition Management. necessary IT programming changes after submission.
To submit your comment online, go to
For the reasons stated in the upgrades to the National Registry.
http://www.regulations.gov, put the
preamble, 48 CFR parts 1519 and 1552 DATES: docket number, FMCSA–2018–0152, in
are amended as set forth below: Effective Date: This interim final rule the keyword box, and click ‘‘Search.’’
is effective June 21, 2018. When the new screen appears, click on
PART 1519—SMALL BUSINESS Public Comment Period: Comments
PROGRAMS the ‘‘Comment Now!’’ button and type
must be received on or before August your comment into the text box on the
20, 2018. following screen. Choose whether you
■ 1. The authority citation for part 1519
continues to read as follows: ADDRESSES: You may submit comments are submitting your comment as an
identified by Docket Number FMCSA– individual or on behalf of a third party
Authority: Sec. 205(c), 63 Stat. 390, as
2018–0152 using any of the following and then submit.
amended, 40 U.S.C. 486(c).
methods: If you submit your comments by mail
1519.203 [Removed and reserved] • Federal eRulemaking Portal: http:// or hand delivery, submit them in an
■ 2. Section 1519.203 is removed and www.regulations.gov. Follow the online unbound format, no larger than 81⁄2 by
reserved. instructions for submitting comments. 11 inches, suitable for copying and
pmangrum on DSK30RV082PROD with RULES
• Mail: Docket Management Facility, electronic filing. If you submit
PART 1552—SOLICITATION U.S. Department of Transportation, 1200 comments by mail and would like to
PROVISIONS AND CONTRACT New Jersey Avenue SE, West Building, know that they reached the facility,
CLAUSES Ground Floor, Room W12–140, please enclose a stamped, self-addressed
Washington, DC 20590–0001. postcard or envelope.
■ 3. The authority citation for part 1552 • Hand Delivery or Courier: West FMCSA will consider all comments
continues to read as follows: Building, Ground Floor, Room W12– and material received during the
VerDate Sep<11>2014 14:07 Jun 20, 2018 Jkt 244001 PO 00000 Frm 00012 Fmt 4700 Sfmt 4700 E:\FR\FM\21JNR1.SGM 21JNR1](https://thefederalregister.org/doc/83_FR_28894/page/1.svg)
![Federal Register / Vol. 83, No. 120 / Thursday, June 21, 2018 / Rules and Regulations 28783
2015, a non-excepted, interstate CDL reached, all retention would be annual commercial fishery quota,
holder without medical certification prohibited through the end of the however the Council recommended, and
status information on the CDLIS motor fishing year. This rule is intended to NMFS is implementing, ACTs under the
vehicle record is designated ‘‘not- conserve and manage the Pacific HG that will trigger a closure of directed
certified’’ to operate a CMV in interstate mackerel stock off the U.S. West Coast. commercial fishing for Pacific mackerel
commerce. After January 30, 2015 and DATES: Effective July 23, 2018 through and incidental harvest provisions. The
through June 21, 2021, a motor carrier June 30, 2019. reason for instituting an ACT and
may use a copy of the driver’s current ADDRESSES: Copies of the report, closing directed fishing at the ACT
medical examiner’s certificate that was ‘‘Pacific Mackerel Biomass Projection instead of all commercial catch at the
submitted to the State for up to 15 days Estimate for USA Management in 2017– HG, is that Pacific mackerel commonly
from the date it was issued as proof of 2018 and 2018–2019’’ may be obtained school with other CPS; the 1,000 mt
medical certification. from the West Coast Regional Office, buffer between the ACT and HG would
* * * * * 501 W Ocean Blvd., Ste. 4200, Long allow for the continued prosecution of
(9) * * * Beach, CA 90802–4250. these other important CPS fisheries after
(ii) Through June 21, 2021, for drivers FOR FURTHER INFORMATION CONTACT:
the ACT for Pacific mackerel is attained.
required to have a CDL, a note relating Joshua Lindsay, West Coast Region, The OFL is the catch level above which
to verification of medical examiner NMFS, (562) 980–4034. overfishing would be occurring and the
listing on the National Registry of ABC is set below the OFL to account for
SUPPLEMENTARY INFORMATION: Under the
Certified Medical Examiners required by scientific uncertainty in the OFL. The
Magnuson-Stevens Fishery
§ 391.23(m)(2). ACL can be set equal to or less than the
Conservation and Management Act
ABC if necessary to ensure overfishing
* * * * * (Magnuson-Stevens Act), 16 U.S.C. 1801
does not occur and serves as the basis
Issued under authority delegated in 49 CFR et seq., NMFS manages the Pacific
to invoke management controls that can
1.87 on: June 15, 2018. mackerel fishery in the U.S. Exclusive
prevent the ACL from being exceeded
Economic Zone off the West Coast in
Raymond P. Martinez, and to correct or mitigate overages of the
accordance with the Coastal Pelagic
Administrator. ACL if they occur, and can be set no
Species (CSP) Fishery Management Plan
[FR Doc. 2018–13314 Filed 6–20–18; 8:45 am] higher than the ABC.
(FMP). The CPS FMP and its The Council recommended, and
BILLING CODE 4910–EX–P implementing regulations require NMFS NMFS is implementing, Pacific
to set annual harvest specifications for mackerel harvest specifications and
the Pacific mackerel fishery based on management measures for both the
DEPARTMENT OF COMMERCE the annual specification framework and 2017–2018 and 2018–2019 fishing years.
control rules in the FMP. The control For the 2017–2018 Pacific mackerel
National Oceanic and Atmospheric rules in the CPS FMP include the HG
Administration fishing year these include an OFL of
control rule, which in conjunction with 30,115 mt, an ABC and ACL of 27,510
the overfishing limit (OFL) and mt, a HG of 26,293 mt, and an ACT of
50 CFR Part 660 acceptable biological catch (ABC) rules, 25,293 mt. For the 2018–2019 Pacific
[Docket No. 170901861–8524–02] are used to manage harvest levels for mackerel fishing year these include an
Pacific mackerel. According to the FMP, OFL of 27,662 mt, an ABC and ACL of
RIN 0648–BH08
the quota for the principal commercial 25,269 mt, a HG of 23,840 mt, and an
Fisheries Off West Coast States; fishery, the HG, is determined using the ACT of 22,840 mt. The Pacific mackerel
Coastal Pelagic Species Fisheries; FMP-specified HG formula. The HG is fishing season runs from July 1 to June
Biennial Specifications based, in large part, on the current 30. These catch specifications are based
estimate of stock biomass. The biomass on the control rules established in the
AGENCY: National Marine Fisheries estimate is an explicit part of the CPS FMP and biomass estimates of
Service (NMFS), National Oceanic and various harvest control rules for Pacific 143,403 mt (2017–2018) and 131,724 mt
Atmospheric Administration (NOAA), mackerel, and as the estimated biomass (2018–2019). These biomass estimates
Commerce. decreases or increases from one year to are the result of the NMFS Southwest
ACTION: Final rule. the next, the resulting allowable catch Fishery Science Center’s Pacific
levels similarly trend. More information mackerel stock assessment completed in
SUMMARY: This final rule implements on the Pacific Fishery Management June 2015, and a subsequent catch-only
annual harvest specifications and Council’s (Council) process for projection estimate completed in June
management measures to establish developing Pacific mackerel harvest 2017. The Council’s Scientific and
allowable catch levels for Pacific specifications and more detail on the Statistical Committee approved the
mackerel for the fishing years 2017– HG control rule are provided in the biomass estimates from the assessment
2018 and 2018–2019. The harvest proposed rule for this action (82 FR and catch-only projection estimate as
guideline (HG) and annual catch target 56204) and are not repeated here. the best available scientific information
(ACT) for the 2017–2018 fishing year are The purpose of this final rule is to for management at its June 2017 meeting
26,293 metric tons (mt) and 25,293 mt, implement these harvest specifications, (see ADDRESSES).
respectively. The HG and ACT for the which include allowable harvest levels Upon the unlikely attainment of the
2018–2019 fishing year are 23,840 mt (ACT, HG, annual catch limit (ACL)), as ACT in either fishing year, directed
and 22,840 mt, respectively. The ACT well as annual catch reference points fishing would close, reserving the
pmangrum on DSK30RV082PROD with RULES
serves as the primary directed (OFL and ABC) that take into difference between the HG and ACT
commercial harvest quotas. If the fishery consideration uncertainty surrounding (1,000 mt) as a set aside for incidental
attains the ACT in either fishing year, the current biomass estimates for Pacific landings in other fisheries and other
the directed fishery will close, reserving mackerel for the 2017–2018 and 2018– sources of mortality. For the remainder
the difference between the HG and ACT 2019 fishing years. As described above, of the fishing year, incidental landings
as a 1,000 mt set-aside for incidental the Pacific mackerel HG control rule is would be constrained to a 45-percent
landings in other fisheries. If the HG is the primary mechanism for setting the incidental catch allowance when Pacific
VerDate Sep<11>2014 14:07 Jun 20, 2018 Jkt 244001 PO 00000 Frm 00021 Fmt 4700 Sfmt 4700 E:\FR\FM\21JNR1.SGM 21JNR1](https://thefederalregister.org/doc/83_FR_28894/page/10.svg)
Document Created: 2018-06-21 01:23:36
Document Modified: 2018-06-21 01:23:36
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Rules and Regulations | |
| Action | Interim final rule; request for comments. | |
| Dates | Effective Date: This interim final rule is effective June 21, 2018. | |
| Contact | Ms. Christine A. Hydock, Chief, Medical Programs Division, Federal Motor Carrier Safety Administration, 1200 New Jersey Avenue SE, Washington, DC 20590-0001, by telephone at 202-366-4001, or by email at [email protected] If you have questions on viewing or submitting material to the docket, contact Docket Services, telephone (202) 366-9826. | |
| FR Citation | 83 FR 28774 | |
| RIN Number | 2126-AC18 | |
| CFR Citation | 49
CFR
383 49 CFR 384 49 CFR 391 | |
| CFR Associated | Administrative Practice and Procedure; Alcohol Abuse; Drug Abuse; Highway Safety; Motor Carriers; Drug Testing; Reporting and Recordkeeping Requirements; Safety and Transportation |
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