81 FR 17065 - Rules of Practice

COMMODITY FUTURES TRADING COMMISSION

Federal Register Volume 81, Issue 59 (March 28, 2016)

Page Range		17065-17065
FR Document		2016-07017

Federal Register, Volume 81 Issue 59 (Monday, March 28, 2016)

[Federal Register Volume 81, Number 59 (Monday, March 28, 2016)]
[Rules and Regulations]
[Page 17065]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2016-07017]


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COMMODITY FUTURES TRADING COMMISSION

17 CFR Part 10


Rules of Practice

CFR Correction

    In Title 17 of the Code of Federal Regulations, Parts 1 to 40, 
revised as of April 1, 2015, on page 386, in Sec.  10.12, paragraph 
(a)(2)(v) is reinstated to read as follows:


Sec.  10.12  Service and filing of documents; form and execution.

    (a) * * *
    (2) * * *
    (v) Service shall be complete at the time of personal service; upon 
deposit in the mail or with a similar commercial package delivery 
service of a properly addressed document for which all postage or 
delivery service fees have been paid; or upon transmission by fax or 
email. Where a party effects service by mail or similar package 
delivery service (but not by fax or email), the time within which the 
party being served may respond shall be extended by five (5) days. 
Service by fax or email shall be permitted at the discretion of the 
Presiding Officer, with the parties' consent. Signed documents that are 
served by email must be in PDF or other non-alterable form.
* * * * *
[FR Doc. 2016-07017 Filed 3-25-16; 8:45 am]
 BILLING CODE 1505-01-D

Federal Register / Vol. 81, No. 59 / Monday, March 28, 2016 / Rules and Regulations 17065

seek CPSC acceptance of their § 1233.1 Scope. served may respond shall be extended
accreditation to test for conformance This part establishes a consumer by five (5) days. Service by fax or email
with the hook-on chair standard. Most product safety standard for portable shall be permitted at the discretion of
of these test laboratories will have hook-on chairs. the Presiding Officer, with the parties’
already been accredited to test for consent. Signed documents that are
conformity to other mandatory juvenile § 1233.2 Requirements for portable hook- served by email must be in PDF or other
on chairs.
product standards, and the only costs to non-alterable form.
them would be the cost of adding the Each portable hook-on chair must
comply with all applicable provisions of * * * * *
hook-on chairs standard to their scope [FR Doc. 2016–07017 Filed 3–25–16; 8:45 am]
of accreditation. For these reasons, the ASTM F1235–15, Standard Consumer
BILLING CODE 1505–01–D
Commission certifies that the NOR Safety Specification for Portable Hook-
amending 16 CFR part 1112 to include On Chairs, approved on May 1, 2015.
the hook-on chairs standard will not The Director of the Federal Register
approves this incorporation by reference DEPARTMENT OF HEALTH AND
have a significant impact on a HUMAN SERVICES
substantial number of small entities. in accordance with 5 U.S.C. 552(a) and
1 CFR part 51. You may obtain a copy
List of Subjects Food and Drug Administration
from ASTM International, 100 Bar
16 CFR Part 1112 Harbor Drive, P.O. Box 0700, West
21 CFR Parts 312 and 320
Conshohocken, PA 19428; http://
Administrative practice and www.astm.org/cpsc.htm. You may [Docket No. FDA–2016–N–0011]
procedure, Audit, Consumer protection, inspect a copy at the Office of the
Reporting and recordkeeping Secretary, U.S. Consumer Product Investigational New Drug Applications
requirements, Third-party conformity Safety Commission, Room 820, 4330 for Biological Products;
assessment body. East West Highway, Bethesda, MD Bioequivalence Regulations; Technical
20814, telephone 301–504–7923, or at Amendment
16 CFR Part 1233
the National Archives and Records AGENCY: Food and Drug Administration,
Consumer protection, Imports, Administration (NARA). For HHS.
Incorporation by reference, Infants and information on the availability of this Final rule; technical
ACTION:
children, Labeling, Law enforcement, material at NARA, call 202–741–6030, amendment.
Toys. or go to: http://www.archives.gov/
For the reasons discussed in the federal_register/code_of_ SUMMARY: The Food and Drug
preamble, the Commission amends title federalregulations/ibr_locations.html. Administration (FDA or Agency) is
16 of the Code of Federal Regulations as Dated: March 22, 2016. amending its regulations to update the
follows: Todd A. Stevenson, address for applicants to submit
Secretary, Consumer Product Safety investigational new drug applications
PART 1112—REQUIREMENTS Commission. (INDs) for biological products regulated
PERTAINING TO THIRD PARTY [FR Doc. 2016–06769 Filed 3–25–16; 8:45 am]
by the Center for Drug Evaluation and
CONFORMITY ASSESSMENT BODIES BILLING CODE 6355–01–P
Research (CDER). FDA is also amending
its regulations on the criteria and
■ 1. The authority citation for part 1112 evidence to assess actual and potential
continues to read as follows: bioequivalence problems
COMMODITY FUTURES TRADING
Authority: Pub. L. 110–314, section 3, 122 (bioequivalence regulations) to correct a
COMMISSION
Stat. 3016, 3017 (2008); 15 U.S.C. 2063. typographical error. FDA is taking this
17 CFR Part 10 action to ensure accuracy and clarity in
■ 2. Amend § 1112.15 by adding and the Agency’s regulations.
reserving paragraph (b)(39) and adding Rules of Practice DATES: This rule is effective March 28,
paragraph (b)(40) to read as follows: 2016.
CFR Correction
§ 1112.15 When can a third party FOR FURTHER INFORMATION CONTACT:
conformity assessment body apply for In Title 17 of the Code of Federal Florine Purdie, Center for Drug
CPSC acceptance for a particular CPSC rule Regulations, Parts 1 to 40, revised as of Evaluation and Research, Food and
or test method? April 1, 2015, on page 386, in § 10.12, Drug Administration, 10903 New
* * * * * paragraph (a)(2)(v) is reinstated to read Hampshire Ave., Bldg. 51, Rm. 6248,
as follows: Silver Spring, MD 20993–0002, 301–
(b) * * *
(40) 16 CFR part 1233, Safety § 10.12 Service and filing of documents; 796–3601.
Standard for Portable Hook-On Chairs. form and execution. SUPPLEMENTARY INFORMATION: FDA is
* * * * * (a) * * * amending 21 CFR 312.140(a)(2) to
(2) * * * update the address for applicants to
■ 3. Add part 1233 to read as follows: (v) Service shall be complete at the submit INDs for biological products
time of personal service; upon deposit regulated by CDER. FDA is amending 21
PART 1233–SAFETY STANDARD FOR in the mail or with a similar commercial CFR 320.33(f)(3) of its bioequivalence
PORTABLE HOOK-ON CHAIRS package delivery service of a properly regulations to correct a typographical
Sec. addressed document for which all error by removing the phrase ‘‘(first-
Lhorne on DSK5TPTVN1PROD with RULES

1233.1 Scope. postage or delivery service fees have class metabolism)’’ and adding in its
1233.2 Requirements for portable hook-on been paid; or upon transmission by fax place ‘‘(first-pass metabolism).’’
chairs. or email. Where a party effects service Publication of this document
Authority: Sec. 104, Pub. L. 110–314, 122 by mail or similar package delivery constitutes final action on these changes
Stat. 3016 (August 14, 2008); Pub. L. 112–28, service (but not by fax or email), the under the Administrative Procedure Act
125 Stat. 273 (August 12, 2011). time within which the party being (5 U.S.C. 553). FDA has determined that

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Document Created: 2016-03-26 00:12:55
Document Modified: 2016-03-26 00:12:55

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
FR Citation		81 FR 17065