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EPA/OCSPP RIN: 2070-AJ65 Publication ID: Spring 2020 
Title: Microorganisms: General Exemptions from Reporting Requirements; Revisions of Recipient Organisms Eligible for Tier I and Tier II Exemptions 
Abstract:

In 1997, EPA promulgated a final rule under section 5 of the Toxic Substances Control Act (TSCA) to establish the notification procedures for review of certain new microorganisms before they are introduced into commerce. "New" microorganisms are those formed by deliberate combinations of genetic material from organisms classified in different taxonomic genera. This review process is designed to prevent unreasonable risk of injury to human health and the environment without imposing unnecessary regulatory burdens on the biotechnology industry. The rule also established TSCA section 5(h)(4) exemptions from full reporting when 10 specific microorganisms are used as the recipient microorganisms for the introduced genetic material and placed requirements on these recipient microorganisms, the introduced genetic material, and the physical containment (40 CFR 725, subpart G). The rule established a mechanism (40 CFR 725.67) for the public to petition the Agency to propose additional recipient microorganisms for such exemptions. Those regulations also described the appropriate supporting information that must be submitted with the petition to provide the EPA with a starting point for determining whether the recipient should be listed as a candidate for the tiered exemption. The EPA received petitions to add Trichoderma reesei and Bacillus amyloliquefaciens to the list of microorganisms that may be used as recipient microorganisms in order to qualify for the exemption from full notification and reporting procedures under the TSCA for new microorganisms that are being manufactured (defined by statute to include import) for introduction into commerce. Based on the EPA's evaluation of these petitions, the EPA made a preliminary determination that certain strains of both microorganisms will not present an unreasonable risk of injury to health or the environment when used as a recipient microorganism provided that certain criteria for the introduced genetic material and the physical containment conditions are met and issued a proposed rule. After considering comments on its proposed exemption, the EPA issued a final action.

 
Agency: Environmental Protection Agency(EPA)  Priority: Substantive, Nonsignificant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Completed Actions 
Major: No  Unfunded Mandates: No 
EO 13771 Designation: Deregulatory 
CFR Citation: 40 CFR 725   
Legal Authority: 15 U.S.C. 2605 Toxic Substances Control Act   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  09/05/2012  77 FR 54499   
Final Rule  03/10/2020  85 FR 13760   
Final Action Effective  04/09/2020 
Additional Information: Docket #:EPA-HQ-OPPT-2011-0740
Regulatory Flexibility Analysis Required: No  Government Levels Affected: Federal 
Small Entities Affected: No  Federalism: No 
Included in the Regulatory Plan: No 
RIN Information URL: http://www.epa.gov/oppt/biotech/index.htm   Public Comment URL: http://www.regulations.gov/#!documentDetail;D=EPA-HQ-OPPT-2011-0740-0001  
Sectors Affected: 325 Chemical Manufacturing 
RIN Data Printed in the FR: No 
Agency Contact:
Rebecca Edelstein
Environmental Protection Agency
Office of Chemical Safety and Pollution Prevention
7406M,
Washington, DC 20460
Phone:202 564-1667
Email: edelstein.rebecca@epa.gov