81 FR 29275 - Over-the-Counter Monograph User Fees: Public Meeting; Request for Comments
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration Federal Register Volume 81, Issue 91 (May 11, 2016)
Food and Drug Administration
Federal Register Volume 81, Issue 91 (May 11, 2016)
| Page Range | 29275-29277 | |
| FR Document | 2016-11098 |
[Federal Register Volume 81, Number 91 (Wednesday, May 11, 2016)] [Notices] [Pages 29275-29277] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2016-11098] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2016-N-1092] Over-the-Counter Monograph User Fees: Public Meeting; Request for Comments AGENCY: Food and Drug Administration, HHS. ACTION: Notice of public meeting; request for comments. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is announcing a public meeting to gather stakeholder input on the potential development of a user-fee program for nonprescription (over-the-counter or OTC) monograph drugs. A user-fee program would provide funding to supplement congressional non-user-fee appropriations, and would support timely and efficient FDA review of the efficacy and safety of ingredients included in or proposed for inclusion in a monograph. FDA invites public comment on a potential OTC monograph user-fee program and also invites suggestions regarding the features such a user-fee program should include. DATES: The public meeting will be held on Friday, June 10, 2016, from 9 a.m. to 5 p.m. EDT. However, depending on the level of public participation, the meeting may be extended or may end early. ADDRESSES: The public meeting will be held at FDA's White Oak Campus, Bldg. 31 Conference Center, 10903 New Hampshire Ave., the Great Room (Rm. 1503A), Silver Spring, MD 20993-0002. Entrance for the public meeting participants (non-FDA employees) is through Building 1, where routine security check procedures will be performed. For parking and security information refer to http://www.fda.gov/aboutfda/workingatfda/buildingsandfacilities/whiteoakcampusinformation/ucm241740.htm. Comments: Regardless of participation at the public meeting, interested persons may submit electronic or written comments regarding this document. To provide adequate time for parties to submit comments before and after the public meeting, the docket will remain open 30 days after the public meeting. You may submit comments as follows: Electronic Submissions Submit electronic comments in the following way:Federal eRulemaking Portal: http://www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to http://www.regulations.gov will be posted to the docket unchanged. Because your comment will be made public, you are solely responsible for ensuring that your comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on http://www.regulations.gov. If you want to submit a comment with confidential information that you do not wish to be made available to the public submit the comment as a written/paper submission and in the manner detailed (see ``Written/Paper Submissions'' and ``Instructions''). Written/Paper Submissions Submit written/paper submissions as follows: Mail/Hand delivery/Courier (for written/paper submissions): Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. For written/paper comments submitted to the Division of Dockets Management, FDA will post your comment, as well as any attachments, except for information submitted, marked and identified, as confidential, if submitted as detailed in ``Instructions.'' Instructions: All submissions received must include the Docket No. FDA-2016-N-1092 for ``Over-the-Counter Monograph User Fees: Public Meeting; Requests for Comments.'' Received comments will be placed in the docket and, except for those submitted as ``Confidential Submissions,'' publicly viewable at http://www.regulations.gov or at the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday. Confidential Submissions--To submit a comment with confidential information that you do not wish to be made publicly available submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on http:// [[Page 29276]] www.regulations.gov. Submit both copies to the Division of Dockets Management. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ``confidential.'' Any information marked as ``confidential'' will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA's posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: http://www.fda.gov/regulatoryinformation/dockets/default.htm. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to http://www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ``Search'' box and follow the prompts and/or go to the Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: Amy Bertha, Office of Executive Programs, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20903-0002, 301-796-1647, email: [email protected]. SUPPLEMENTARY INFORMATION: I. Background FDA is announcing a public meeting to obtain input on a potential OTC monograph user-fee program. The Prescription Drug User Fee Act (PDUFA) and other FDA user-fee programs for medical products provide vital resources that have enabled more timely evaluation of the safety and efficacy of many prescription drugs, biologics and devices, with consequent benefits to public health through the expanded availability of products to treat and manage a wide variety of conditions. However, no user-fee program exists for hundreds of thousands of drug products marketed under OTC drug monographs. Millions of American consumers every year use monograph drug products to self-manage numerous conditions. The efficacy and safety of these drugs is important to public health, but FDA is critically under-resourced in this regulatory area. In the United States, OTC drugs are marketed in two different ways--under an approved marketing application (new drug application (NDA) or abbreviated new drug application (ANDA)) or under the OTC monograph system, which was set up to review the safety and efficacy of drug products that were marketed OTC in the United States prior to the current statutory NDA process. When sponsors submit marketing applications, FDA reviews these applications and approves those drugs that are found to be safe and effective under their proposed conditions of use with benefits that outweigh their risks. However, at the time of establishment of the statutory efficacy requirement, there were hundreds of thousands of OTC products on the market. Withdrawing all those products and requiring submission of a new drug application for each one was undesirable for public health, and would have resulted in an overwhelming number of individual applications for review. Instead, in 1972, FDA established the OTC drug review process. In that process, expert advisory review panels were established to evaluate evidence of safety and efficacy for ingredients in broad therapeutic classes of OTC drug products. These panels reviewed data submissions and provided reports to FDA. Those reports made recommendations regarding whether or not the ingredients were ``generally recognized as safe and effective (GRASE)'' for use in self-treatment. The review panels also reviewed claims and recommended appropriate labeling. Based on the panels' reviews, FDA published in the Federal Register advanced notices of proposed rulemaking and, after additional Agency review and public comment, tentative final monographs. Subsequently, final regulations in the form of individual drug monographs were established for various therapeutic areas; these monographs establish conditions of use under which ingredients are considered GRASE for inclusion in an OTC drug. Conditions of use can include, for example, indications for use, dosage form, and route of administration. Products that conform to all applicable regulations, including all aspects of the relevant monograph, will be GRASE and not misbranded if marketed without an approved marketing application. GRASE determinations were made, and monographs proposed and finalized, for many ingredients for many drug products. However, the process has not been completed for all ingredients, nor for all OTC conditions of use. In many cases, the data submitted to the advisory panels were inadequate for a final GRASE determination; these ingredients are referred to as ``Category III'' ingredients in OTC products. Many products containing Category III ingredients without a GRASE determination continue to be marketed. By contrast, ingredients with a final determination of ``not GRASE'' need an approved marketing application to be legally marketed. The OTC monograph drug review process remains one of the largest and most complex regulatory programs ever undertaken at FDA. There are approximately 88 simultaneous rulemakings in 26 broad therapeutic areas encompassing hundreds of thousands of products. There are approximately 800 active ingredients for over 1,400 different therapeutic uses. FDA needs additional resources to work toward finalization of the monograph review process and to address safety issues in a more efficient and timely manner. Additional resources would also better enable the Agency to consider innovations for drug products containing monograph ingredients, such as the development of new dosage forms for ingredients under existing monographs. There are some important differences between marketing through approved applications and marketing under the monographs. NDAs and ANDAs are product-based; an application typically is submitted with data for a single drug product to be marketed by a single sponsor, and that application will be approved or not approved. By contrast, the monograph system is ingredient-based; numerous sponsors may make the same ingredient for the same use, and all may market drug products made with this ingredient as long as they comply with all applicable regulations, including the conditions of the monograph. Sponsors of monograph drugs are not required to seek FDA approval prior to marketing a product under the monograph. In addition, the monograph system, where ingredients are determined to be GRASE or not, is a public process. Data are submitted to public dockets, and anyone may provide input. By contrast, while FDA typically makes NDA information public after approval of a product, it generally cannot do so before. At this time, once a monograph has been established, additional rulemaking is required for changes to that monograph. FDA is working on multiple policy reforms to streamline and modernize the monograph system; those policy reforms are not the topic of this public meeting. Funds from other user-fee programs cannot be used to fund monograph activities, and FDA receives [[Page 29277]] very few resources that it can allocate to monograph review work. The potential benefits of additional resources from a monograph user-fee program include benefits to public health and sponsors of monograph drug products, such as the following: Ability to address safety issues of currently marketed products in an efficient and timely manner. Timely determination on the safety and efficacy of monograph ingredients under the conditions of the monograph, helping to assure appropriate marketing of thousands of nonprescription products used daily by U.S. consumers. Increased availability of certain monograph product innovations proposed by industry. Streamlined ability to update monographs to allow modern testing methods in several areas, potentially reducing the need for animal testing, and simplifying and speeding product development. Development of information technology infrastructure to speed numerous parts of the monograph review process, and enable a modern robust system for submission of materials and archiving of documents. Development of a modern, useful, and transparent FDA monograph Web site to provide the public and industry with access to important information. Ability to hold more public meetings on important monograph issues. Increased ability of FDA to respond to monograph-related concerns and questions from the public and industry. Establishment of additional infrastructure for the efficient continued conduct of monograph activities in the longer term. II. Purpose of Public Meeting The purpose of the meeting is to obtain input from industry and other interested stakeholders regarding a potential OTC monograph user- fee program. There are several factors that FDA considers important in developing a user-fee program. First, to achieve a program's goals of efficient and timely oversight of a category of products, FDA must be able to rely on a stable and predictable source of adequate funding. Funding sources that result in unpredictable revenue cause uncertainty about FDA's ability to continue supporting activities over time which disrupts the Agency's regulatory operations and contributes to difficulties in conducting long-range planning. Second, the assessment of fees can create certain incentives or disincentives for the activity that is the subject of the fee. For example, a sponsor who currently has an unmarketed product has an incentive to pay a fee to seek FDA approval to market the product. However, once the product is approved and marketed, there is less incentive to pay a fee for additional specific activities regarding the product that are otherwise not required. If those activities are important from a public health perspective, assessing a fee for them would be undesirable because the fee could discourage entities to undertake those activities. With these considerations in mind, FDA seeks input on the following questions and welcomes any other relevant information the public would like to share. What types of user fees (e.g. product listing fees, facility fees, application fees, other types of fees) might be appropriate for a potential monograph user-fee program? Consider the following in your answer: [cir] For monograph products (unlike for products currently covered by user-fee programs), premarket applications are not generally submitted, and thus the approach regarding application-based fees might be expected to be different for a monograph user fee program compared to other user fee programs. [cir] Desirable industry activities or behavior that might be discouraged by the assessment of fees. [cir] The stability and predictability of the funding provided by the user-fee type. In conjunction with receiving user fees, FDA typically commits to certain performance goals related to the Agency's activities with respect to the relevant products. What types of performance goals might be important to consider from a public health and sponsor perspective? What parameters could be measured to gauge the success of a user-fee program? III. Meeting Attendance and Participation The public meeting is free and seating will be on a first-come, first-served basis. FDA is seeking participation (i.e., attendance and oral presentations) at the public meeting by all interested parties. In general the meeting format may include, but will not be limited to, presentations by FDA staff, scientific and academic experts, health care professionals, representatives of patient and consumer advocacy groups, and representatives of the OTC monograph industry. If you wish to attend the public meeting either in person or by viewing the web cast, FDA asks that you please register through Eventbrite by Tuesday, May 31, 2016, in order for FDA to estimate the number of attendees (https://www.eventbrite.com/e/over-the-counter-monograph-user-fees-public-meeting-tickets-21565448838). If you wish to make an oral presentation at the public meeting, you must register through Eventbrite by Tuesday, May 31, 2016 (https://www.eventbrite.com/e/over-the-counter-monograph-user-fees-public-meeting-tickets-21565448838). FDA encourages individuals and organizations with common interests to coordinate and give a joint, consolidated presentation. FDA will try to accommodate all persons who wish to make a presentation; however, FDA may limit both the number of participants from individual organizations and the total number of attendees based on space and time limitations. FDA will notify registered presenters of their scheduled presentation times. Persons registered to speak should check in before the meeting and are encouraged to arrive early to ensure their designated order of presentation. Participants who are not present when called may not be permitted to speak at a later time. FDA will post an agenda of the public meeting and other background material at least 3 days before the public meeting and additional information will be available at: http://www.fda.gov/Drugs/NewsEvents/ucm499390.htm. This public meeting will be web cast and the URL will be posted at http://www.fda.gov/Drugs/NewsEvents/ucm499390.htm at least 1 day before the meeting. A video record of the public meeting will be available at the same Web site address for 1 year. If you need special accommodations because of disability, please contact Amy Bertha (see FOR FURTHER INFORMATION CONTACT) no later than Friday, May 27, 2016. IV. Transcripts Please be advised that as soon as a transcript is available, it will be accessible at http://www.regulations.gov. It may be viewed at the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD. A transcript will also be available in either hardcopy or on CD-ROM after submission of a Freedom of Information request. The Freedom of Information office address is available on the Agency's Web site at http://www.fda.gov. Dated: May 5, 2016. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2016-11098 Filed 5-10-16; 8:45 am] BILLING CODE 4164-01-P
![Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 2016 / Notices 29275
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1—Continued
Number of Average
Number of Total annual
FD&C Act sections 512 (b)(2) and (n)(1) FDA Form responses per burden per Total hours
respondents responses
respondent response
Phased Review with Administrative
ANADA ................................................. 356v 3 5 15 31.8 477
Total .................................................. ........................ ........................ ........................ ........................ ........................ 3,339
1 There are no capital costs or operating and maintenance costs associated with this collection of information.
We base our estimates on our features such a user-fee program should identifies you in the body of your
experience with ANADA submissions include. comments, that information will be
and requests for phased review. We DATES: The public meeting will be held posted on http://www.regulations.gov.
estimate that we will receive 21 ANADA on Friday, June 10, 2016, from 9 a.m. to • If you want to submit a comment
submissions per year over the next three 5 p.m. EDT. However, depending on the with confidential information that you
years and that three of those level of public participation, the do not wish to be made available to the
submissions will request phased review. meeting may be extended or may end public submit the comment as a written/
We estimate that each applicant that early. paper submission and in the manner
uses the phased review process will detailed (see ‘‘Written/Paper
ADDRESSES: The public meeting will be
have approximately five phased reviews Submissions’’ and ‘‘Instructions’’).
held at FDA’s White Oak Campus, Bldg.
per application. We estimate that an 31 Conference Center, 10903 New Written/Paper Submissions
applicant will take approximately 159 Hampshire Ave., the Great Room (Rm.
hours to prepare either an ANADA or Submit written/paper submissions as
1503A), Silver Spring, MD 20993–0002. follows:
the estimated 5 ANADA phased review Entrance for the public meeting • Mail/Hand delivery/Courier (for
submissions and the administrative participants (non-FDA employees) is written/paper submissions): Division of
ANADA. through Building 1, where routine Dockets Management (HFA–305), Food
Dated: May 5, 2016. security check procedures will be and Drug Administration, 5630 Fishers
Leslie Kux, performed. For parking and security Lane, Rm. 1061, Rockville, MD 20852.
Associate Commissioner for Policy. information refer to http://www.fda.gov/ • For written/paper comments
[FR Doc. 2016–11114 Filed 5–10–16; 8:45 am] aboutfda/workingatfda/ submitted to the Division of Dockets
BILLING CODE 4164–01–P buildingsandfacilities/ Management, FDA will post your
whiteoakcampusinformation/ comment, as well as any attachments,
ucm241740.htm. except for information submitted,
DEPARTMENT OF HEALTH AND Comments: Regardless of marked and identified, as confidential,
HUMAN SERVICES participation at the public meeting, if submitted as detailed in
interested persons may submit ‘‘Instructions.’’
Food and Drug Administration electronic or written comments Instructions: All submissions received
regarding this document. To provide must include the Docket No. FDA–
[Docket No. FDA–2016–N–1092] adequate time for parties to submit 2016–N–1092 for ‘‘Over-the-Counter
comments before and after the public Monograph User Fees: Public Meeting;
Over-the-Counter Monograph User meeting, the docket will remain open 30 Requests for Comments.’’ Received
Fees: Public Meeting; Request for days after the public meeting. comments will be placed in the docket
Comments You may submit comments as and, except for those submitted as
follows: ‘‘Confidential Submissions,’’ publicly
AGENCY: Food and Drug Administration, viewable at http://www.regulations.gov
HHS. Electronic Submissions or at the Division of Dockets
ACTION: Notice of public meeting; Submit electronic comments in the Management between 9 a.m. and 4 p.m.,
request for comments. following way: Monday through Friday.
• Federal eRulemaking Portal: http:// • Confidential Submissions—To
SUMMARY: The Food and Drug www.regulations.gov. Follow the submit a comment with confidential
Administration (FDA) is announcing a instructions for submitting comments. information that you do not wish to be
public meeting to gather stakeholder Comments submitted electronically, made publicly available submit your
input on the potential development of a including attachments, to http:// comments only as a written/paper
user-fee program for nonprescription www.regulations.gov will be posted to submission. You should submit two
(over-the-counter or OTC) monograph the docket unchanged. Because your copies total. One copy will include the
drugs. A user-fee program would comment will be made public, you are information you claim to be confidential
provide funding to supplement solely responsible for ensuring that your with a heading or cover note that states
congressional non-user-fee comment does not include any ‘‘THIS DOCUMENT CONTAINS
appropriations, and would support confidential information that you or a CONFIDENTIAL INFORMATION.’’ The
mstockstill on DSK3G9T082PROD with NOTICES
timely and efficient FDA review of the third party may not wish to be posted, Agency will review this copy, including
efficacy and safety of ingredients such as medical information, your or the claimed confidential information, in
included in or proposed for inclusion in anyone else’s Social Security number, or its consideration of comments. The
a monograph. FDA invites public confidential business information, such second copy, which will have the
comment on a potential OTC as a manufacturing process. Please note claimed confidential information
monograph user-fee program and also that if you include your name, contact redacted/blacked out, will be available
invites suggestions regarding the information, or other information that for public viewing and posted on http://
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![Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 2016 / Notices 29277
very few resources that it can allocate to sponsor who currently has an FDA to estimate the number of
monograph review work. unmarketed product has an incentive to attendees (https://www.eventbrite.com/
The potential benefits of additional pay a fee to seek FDA approval to e/over-the-counter-monograph-user-
resources from a monograph user-fee market the product. However, once the fees-public-meeting-tickets-
program include benefits to public product is approved and marketed, 21565448838).
health and sponsors of monograph drug there is less incentive to pay a fee for If you wish to make an oral
products, such as the following: additional specific activities regarding presentation at the public meeting, you
• Ability to address safety issues of the product that are otherwise not must register through Eventbrite by
currently marketed products in an required. If those activities are Tuesday, May 31, 2016 (https://
efficient and timely manner. important from a public health www.eventbrite.com/e/over-the-counter-
• Timely determination on the safety perspective, assessing a fee for them monograph-user-fees-public-meeting-
and efficacy of monograph ingredients would be undesirable because the fee tickets-21565448838). FDA encourages
under the conditions of the monograph, could discourage entities to undertake individuals and organizations with
helping to assure appropriate marketing those activities. With these common interests to coordinate and give
of thousands of nonprescription considerations in mind, FDA seeks a joint, consolidated presentation. FDA
products used daily by U.S. consumers. input on the following questions and will try to accommodate all persons
• Increased availability of certain welcomes any other relevant who wish to make a presentation;
monograph product innovations information the public would like to however, FDA may limit both the
proposed by industry. share. number of participants from individual
• Streamlined ability to update • What types of user fees (e.g. product organizations and the total number of
monographs to allow modern testing listing fees, facility fees, application attendees based on space and time
methods in several areas, potentially fees, other types of fees) might be limitations. FDA will notify registered
reducing the need for animal testing, appropriate for a potential monograph presenters of their scheduled
and simplifying and speeding product user-fee program? Consider the presentation times. Persons registered to
development. following in your answer: speak should check in before the
• Development of information Æ For monograph products (unlike for meeting and are encouraged to arrive
technology infrastructure to speed products currently covered by user-fee early to ensure their designated order of
numerous parts of the monograph programs), premarket applications are presentation. Participants who are not
review process, and enable a modern not generally submitted, and thus the present when called may not be
robust system for submission of approach regarding application-based permitted to speak at a later time. FDA
materials and archiving of documents. fees might be expected to be different will post an agenda of the public
• Development of a modern, useful, for a monograph user fee program meeting and other background material
and transparent FDA monograph Web compared to other user fee programs. at least 3 days before the public meeting
site to provide the public and industry Æ Desirable industry activities or and additional information will be
with access to important information. behavior that might be discouraged by available at: http://www.fda.gov/Drugs/
• Ability to hold more public the assessment of fees. NewsEvents/ucm499390.htm.
meetings on important monograph Æ The stability and predictability of This public meeting will be web cast
issues. the funding provided by the user-fee and the URL will be posted at http://
• Increased ability of FDA to respond type. www.fda.gov/Drugs/NewsEvents/
to monograph-related concerns and • In conjunction with receiving user ucm499390.htm at least 1 day before the
questions from the public and industry. fees, FDA typically commits to certain meeting. A video record of the public
• Establishment of additional performance goals related to the meeting will be available at the same
infrastructure for the efficient continued Agency’s activities with respect to the Web site address for 1 year. If you need
conduct of monograph activities in the relevant products. What types of special accommodations because of
longer term. performance goals might be important to disability, please contact Amy Bertha
consider from a public health and (see FOR FURTHER INFORMATION CONTACT)
II. Purpose of Public Meeting
sponsor perspective? What parameters no later than Friday, May 27, 2016.
The purpose of the meeting is to could be measured to gauge the success
obtain input from industry and other of a user-fee program? IV. Transcripts
interested stakeholders regarding a Please be advised that as soon as a
potential OTC monograph user-fee III. Meeting Attendance and
Participation transcript is available, it will be
program. There are several factors that accessible at http://
FDA considers important in developing The public meeting is free and seating www.regulations.gov. It may be viewed
a user-fee program. First, to achieve a will be on a first-come, first-served at the Division of Dockets Management
program’s goals of efficient and timely basis. FDA is seeking participation (i.e., (HFA–305), Food and Drug
oversight of a category of products, FDA attendance and oral presentations) at the Administration, 5630 Fishers Lane, Rm.
must be able to rely on a stable and public meeting by all interested parties. 1061, Rockville, MD. A transcript will
predictable source of adequate funding. In general the meeting format may also be available in either hardcopy or
Funding sources that result in include, but will not be limited to, on CD–ROM after submission of a
unpredictable revenue cause presentations by FDA staff, scientific Freedom of Information request. The
uncertainty about FDA’s ability to and academic experts, health care Freedom of Information office address is
continue supporting activities over time professionals, representatives of patient
mstockstill on DSK3G9T082PROD with NOTICES
available on the Agency’s Web site at
which disrupts the Agency’s regulatory and consumer advocacy groups, and http://www.fda.gov.
operations and contributes to representatives of the OTC monograph
difficulties in conducting long-range industry. If you wish to attend the Dated: May 5, 2016.
planning. Second, the assessment of fees public meeting either in person or by Leslie Kux,
can create certain incentives or viewing the web cast, FDA asks that you Associate Commissioner for Policy.
disincentives for the activity that is the please register through Eventbrite by [FR Doc. 2016–11098 Filed 5–10–16; 8:45 am]
subject of the fee. For example, a Tuesday, May 31, 2016, in order for BILLING CODE 4164–01–P
VerDate Sep<11>2014 17:20 May 10, 2016 Jkt 238001 PO 00000 Frm 00029 Fmt 4703 Sfmt 9990 E:\FR\FM\11MYN1.SGM 11MYN1](https://thefederalregister.org/doc/81_FR_29366/page/3.svg)
Document Created: 2016-05-11 01:12:18
Document Modified: 2016-05-11 01:12:18
| 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 | Notices | |
| Action | Notice of public meeting; request for comments. | |
| Dates | The public meeting will be held on Friday, June 10, 2016, from 9 a.m. to 5 p.m. EDT. However, depending on the level of public participation, the meeting may be extended or may end early. | |
| Contact | Amy Bertha, Office of Executive Programs, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20903-0002, 301-796-1647, email: [email protected] | |
| FR Citation | 81 FR 29275 |
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