Regulation of Fuels and Fuel Additives: Identification of Additional Qualifying Renewable Fuel Pathways Under the Renewable Fuel Standard Program, 13009-13010 [2012-5256]

Download as PDF tkelley on DSK3SPTVN1PROD with RULES Federal Register / Vol. 77, No. 43 / Monday, March 5, 2012 / Rules and Regulations representatives are prohibited from marketing to medical, pharmacy, nursing and other health profession students, including residents. Exceptions may be permitted when approved by, and conducted in the presence of, the staff member providing clinical supervision. (4) Attendance at conferences. A pharmaceutical company representative may not attend a medical center conference where information regarding individual patients is discussed or presented. (5) Patient care areas. Pharmaceutical company representatives generally may not wait for scheduled appointments or make presentations in patient-care areas, but may briefly travel through them, when necessary, to meet in a staff member’s office. Patient-care areas include, but are not limited to: (i) Patient rooms and ward areas where patients may be encountered; (ii) Clinic examination rooms; (iii) Nurses stations; (iv) Intensive care units; (v) Operating room suites; (vi) Urgent care centers; (vii) Emergency rooms (but not staff offices that may be located in them); or (viii) Ambulatory treatment centers. (6) Distribution of materials. Pharmaceutical company representatives may only distribute materials on-site at the time and location of a scheduled appointment or educational program. In no circumstances may materials be left in patient care areas. (i) Non-compliance. (1) General. The visiting privileges of a pharmaceutical company representative or multiple representatives may be limited, suspended, or revoked by the written order of the Director of the VA medical center of jurisdiction if the Director determines the pharmaceutical company representative(s) failed to comply with the requirements of this section. (2) Notice of interim action. The Director will notify the pharmaceutical company representative of the noncompliance and of the Director’s interim action under paragraph (i)(4) of this section. The Director will also notify the supervisor of the pharmaceutical company representative(s) if there have been multiple instances of misconduct. The notice will offer 30 days to provide a response; however, the interim action will be enforced effective the date of the notice. (3) Final written order. At the end of the 30-day period for a response, or after the Director receives a timely response, VerDate Mar<15>2010 16:55 Mar 02, 2012 Jkt 226001 the Director will issue to the pharmaceutical company representative and supervisor a final written order either confirming the action taken as indicated in the notice, or specifying another action to be taken under paragraph (i)(4) of this section. The written order may also state that the Director has determined that no further action is required. Any final written order issued by the Director shall include a summary of the circumstances of the violation, a listing of the specific provisions of this section that the pharmaceutical company representative(s) violated, and the bases for the Director’s determination regarding the appropriate action. Notice concerning a final written order suspending or permanently revoking the visiting privileges of multiple pharmaceutical company representatives shall include specific notice concerning the right to review of the Director’s order by the Under Secretary for Health. (4) Actions. Actions that may be imposed under this section include limitation, suspension, or permanent revocation of visiting privileges at one or more VA medical facilities. In determining the appropriate action, the Director shall consider the requirements of this section, the circumstances of the improper conduct, any prior acts of misconduct by the same pharmaceutical company representative, any response submitted by the pharmaceutical company representative or their supervisor under paragraph (i)(2) of this section, and any prior written orders issued or other actions taken with respect to similar acts of misconduct. (5) Review. The pharmaceutical company may request the Under Secretary’s review within 30 days of the date of the Director’s final written order by submitting a written request to the Director. The Director shall forward the initial notice, any response, the final written order, and the request for review to the Under Secretary for a final VA decision. VA will enforce the Director’s final written order while it is under review by the Under Secretary. The Director will provide the individual who made the request written notice of the Under Secretary’s decision. (Authority: 38 U.S.C. 501) [FR Doc. 2012–5279 Filed 3–2–12; 8:45 am] BILLING CODE 8320–01–P PO 00000 Frm 00021 Fmt 4700 Sfmt 4700 13009 ENVIRONMENTAL PROTECTION AGENCY 40 CFR Part 80 [EPA–HQ–OAR–2011–0542; FRL–9642–3] RIN 2060–AR07 Regulation of Fuels and Fuel Additives: Identification of Additional Qualifying Renewable Fuel Pathways Under the Renewable Fuel Standard Program Environmental Protection Agency (EPA). ACTION: Withdrawal of direct final rule. AGENCY: EPA published a direct final rule on January 5, 2012 to amend the Renewable Fuel Standard program regulations. Because EPA received adverse comment, we are withdrawing the direct final rule. DATES: Effective March 5, 2012, EPA withdraws the direct final rule published at 77 FR 700, on January 5, 2012. FOR FURTHER INFORMATION CONTACT: Vincent Camobreco, Office of Transportation and Air Quality (MC6401A), Environmental Protection Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460; telephone number: (202) 564–9043; fax number: (202) 564–1686; email address: camobreco.vincent@epa.gov. SUMMARY: EPA published a direct final rule on January 5, 2012 (77 FR 700) to amend the Renewable Fuel Standard program regulations. The amendments would have expanded Table 1 of § 80.1426 to identify additional renewable fuel production pathways and pathway components that could be used in producing qualifying renewable fuel under the Renewable Fuel Standard program. We stated in that direct final rule that if we received adverse comment by February 6, 2012, that we would publish a timely withdrawal in the Federal Register. We subsequently received adverse comment on several of the changes included in the revised Table 1 of § 80.1426. Since the regulatory amendment in the direct final rule was a single Table including all changes, withdrawal based on the adverse comments we have received requires withdrawal of the entire revised Table. EPA intends to address all comments in a subsequent final action, which will be based on the parallel proposed rule also published on January 5, 2012 (77 FR 462). As stated in the direct final rule and the parallel proposed rule, we will not SUPPLEMENTARY INFORMATION: E:\FR\FM\05MRR1.SGM 05MRR1 13010 Federal Register / Vol. 77, No. 43 / Monday, March 5, 2012 / Rules and Regulations institute a second comment period on this action. Dated: February 27, 2012. Lisa P. Jackson, Administrator. Accordingly, the regulatory amendments published on January 5, 2012 (77 FR 700) are withdrawn as of March 5, 2012. [FR Doc. 2012–5256 Filed 3–2–12; 8:45 am] BILLING CODE 6560–50–P DEPARTMENT OF HOMELAND SECURITY Federal Emergency Management Agency 44 CFR Part 64 [Docket ID FEMA–2012–0003; Internal Agency Docket No. FEMA–8221] Suspension of Community Eligibility Federal Emergency Management Agency, DHS. ACTION: Final rule. AGENCY: This rule identifies communities where the sale of flood insurance has been authorized under the National Flood Insurance Program (NFIP) that are scheduled for suspension on the effective dates listed within this rule because of noncompliance with the floodplain management requirements of the program. If the Federal Emergency Management Agency (FEMA) receives documentation that the community has adopted the required floodplain management measures prior to the effective suspension date given in this rule, the suspension will not occur and a notice of this will be provided by publication in the Federal Register on a subsequent date. DATES: Effective Dates: The effective date of each community’s scheduled suspension is the third date (‘‘Susp.’’) listed in the third column of the following tables. FOR FURTHER INFORMATION CONTACT: If you want to determine whether a particular community was suspended on the suspension date or for further information, contact David Stearrett, Federal Insurance and Mitigation Administration, Federal Emergency Management Agency, 500 C Street SW., Washington, DC 20472, (202) 646–2953. SUPPLEMENTARY INFORMATION: The NFIP enables property owners to purchase Federal flood insurance that is not tkelley on DSK3SPTVN1PROD with RULES SUMMARY: VerDate Mar<15>2010 16:55 Mar 02, 2012 Jkt 226001 otherwise generally available from private insurers. In return, communities agree to adopt and administer local floodplain management measures aimed at protecting lives and new construction from future flooding. Section 1315 of the National Flood Insurance Act of 1968, as amended, 42 U.S.C. 4022, prohibits the sale of NFIP flood insurance unless an appropriate public body adopts adequate floodplain management measures with effective enforcement measures. The communities listed in this document no longer meet that statutory requirement for compliance with program regulations, 44 CFR part 59. Accordingly, the communities will be suspended on the effective date in the third column. As of that date, flood insurance will no longer be available in the community. We recognize that some of these communities may adopt and submit the required documentation of legally enforceable floodplain management measures after this rule is published but prior to the actual suspension date. These communities will not be suspended and will continue to be eligible for the sale of NFIP flood insurance. A notice withdrawing the suspension of such communities will be published in the Federal Register. In addition, FEMA publishes a Flood Insurance Rate Map (FIRM) that identifies the Special Flood Hazard Areas (SFHAs) in these communities. The date of the FIRM, if one has been published, is indicated in the fourth column of the table. No direct Federal financial assistance (except assistance pursuant to the Robert T. Stafford Disaster Relief and Emergency Assistance Act not in connection with a flood) may be provided for construction or acquisition of buildings in identified SFHAs for communities not participating in the NFIP and identified for more than a year on FEMA’s initial FIRM for the community as having flood-prone areas (section 202(a) of the Flood Disaster Protection Act of 1973, 42 U.S.C. 4106(a), as amended). This prohibition against certain types of Federal assistance becomes effective for the communities listed on the date shown in the last column. The Administrator finds that notice and public comment procedures under 5 U.S.C. 553(b), are impracticable and unnecessary because communities listed in this final rule have been adequately notified. Each community receives 6-month, 90-day, and 30-day notification letters addressed to the Chief Executive Officer stating that the community will be PO 00000 Frm 00022 Fmt 4700 Sfmt 4700 suspended unless the required floodplain management measures are met prior to the effective suspension date. Since these notifications were made, this final rule may take effect within less than 30 days. National Environmental Policy Act. This rule is categorically excluded from the requirements of 44 CFR part 10, Environmental Considerations. No environmental impact assessment has been prepared. Regulatory Flexibility Act. The Administrator has determined that this rule is exempt from the requirements of the Regulatory Flexibility Act because the National Flood Insurance Act of 1968, as amended, Section 1315, 42 U.S.C. 4022, prohibits flood insurance coverage unless an appropriate public body adopts adequate floodplain management measures with effective enforcement measures. The communities listed no longer comply with the statutory requirements, and after the effective date, flood insurance will no longer be available in the communities unless remedial action takes place. Regulatory Classification. This final rule is not a significant regulatory action under the criteria of section 3(f) of Executive Order 12866 of September 30, 1993, Regulatory Planning and Review, 58 FR 51735. Executive Order 13132, Federalism. This rule involves no policies that have federalism implications under Executive Order 13132. Executive Order 12988, Civil Justice Reform. This rule meets the applicable standards of Executive Order 12988. Paperwork Reduction Act. This rule does not involve any collection of information for purposes of the Paperwork Reduction Act, 44 U.S.C. 3501 et seq. List of Subjects in 44 CFR Part 64 Flood insurance, Floodplains. Accordingly, 44 CFR part 64 is amended as follows: PART 64—[AMENDED] 1. The authority citation for part 64 continues to read as follows: ■ Authority: 42 U.S.C. 4001 et seq.; Reorganization Plan No. 3 of 1978, 3 CFR, 1978 Comp.; p. 329; E.O. 12127, 44 FR 19367, 3 CFR, 1979 Comp.; p. 376. § 64.6 [Amended] 2. The tables published under the authority of § 64.6 are amended as follows: ■ E:\FR\FM\05MRR1.SGM 05MRR1

Agencies

[Federal Register Volume 77, Number 43 (Monday, March 5, 2012)]
[Rules and Regulations]
[Pages 13009-13010]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-5256]


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ENVIRONMENTAL PROTECTION AGENCY

40 CFR Part 80

[EPA-HQ-OAR-2011-0542; FRL-9642-3]
RIN 2060-AR07


Regulation of Fuels and Fuel Additives: Identification of 
Additional Qualifying Renewable Fuel Pathways Under the Renewable Fuel 
Standard Program

AGENCY: Environmental Protection Agency (EPA).

ACTION: Withdrawal of direct final rule.

-----------------------------------------------------------------------

SUMMARY: EPA published a direct final rule on January 5, 2012 to amend 
the Renewable Fuel Standard program regulations. Because EPA received 
adverse comment, we are withdrawing the direct final rule.

DATES: Effective March 5, 2012, EPA withdraws the direct final rule 
published at 77 FR 700, on January 5, 2012.

FOR FURTHER INFORMATION CONTACT: Vincent Camobreco, Office of 
Transportation and Air Quality (MC6401A), Environmental Protection 
Agency, 1200 Pennsylvania Ave. NW., Washington, DC 20460; telephone 
number: (202) 564-9043; fax number: (202) 564-1686; email address: 
camobreco.vincent@epa.gov.

SUPPLEMENTARY INFORMATION: EPA published a direct final rule on January 
5, 2012 (77 FR 700) to amend the Renewable Fuel Standard program 
regulations. The amendments would have expanded Table 1 of Sec.  
80.1426 to identify additional renewable fuel production pathways and 
pathway components that could be used in producing qualifying renewable 
fuel under the Renewable Fuel Standard program. We stated in that 
direct final rule that if we received adverse comment by February 6, 
2012, that we would publish a timely withdrawal in the Federal 
Register. We subsequently received adverse comment on several of the 
changes included in the revised Table 1 of Sec.  80.1426. Since the 
regulatory amendment in the direct final rule was a single Table 
including all changes, withdrawal based on the adverse comments we have 
received requires withdrawal of the entire revised Table. EPA intends 
to address all comments in a subsequent final action, which will be 
based on the parallel proposed rule also published on January 5, 2012 
(77 FR 462).
    As stated in the direct final rule and the parallel proposed rule, 
we will not

[[Page 13010]]

institute a second comment period on this action.

    Dated: February 27, 2012.
Lisa P. Jackson,
Administrator.
    Accordingly, the regulatory amendments published on January 5, 2012 
(77 FR 700) are withdrawn as of March 5, 2012.

[FR Doc. 2012-5256 Filed 3-2-12; 8:45 am]
BILLING CODE 6560-50-P
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