Home/CFR/Title 40/Part 725
FEDERAL · 40 CFR

Part 725 — Reporting Requirements and Review Processes for Microorganisms

75 sections · Title 40: Protection of Environment

§ 725.1Scope and purpose.
§ 725.3Definitions.
§ 725.8Coverage of this part.
§ 725.12Identification of microorganisms for Inventory and other listing purposes.
§ 725.15Determining applicability when microorganism identity or use is confidential or uncertain.
§ 725.17Consultation with EPA.
§ 725.20Scope and purpose.
§ 725.25General administrative requirements.
§ 725.27Submissions.
§ 725.28Notice that submission is not required.
§ 725.29EPA acknowledgement of receipt of submission.
§ 725.32Errors in the submission.
§ 725.33Incomplete submissions.
§ 725.36New information.
§ 725.40Notice in the Federal Register.
§ 725.50EPA review.
§ 725.54Suspension of the review period.
§ 725.56Extension of the review period.
§ 725.60Withdrawal of submission by the submitter.
§ 725.65Recordkeeping.
§ 725.67Applications to exempt new microorganisms from this part.
§ 725.70Compliance.
§ 725.75Inspections.
§ 725.80General provisions for confidentiality claims.
§ 725.88Uses of a microorganism.
§ 725.95Public file.
§ 725.100Scope and purpose.
§ 725.105Persons who must report.
§ 725.110Persons not subject to this subpart.
§ 725.150Procedural requirements for this subpart.
§ 725.155Information to be included in the MCAN.
§ 725.160Submission of health and environmental effects data.
§ 725.170EPA review of the MCAN.
§ 725.190Notice of commencement of manufacture or import.
§ 725.200Scope and purpose.
§ 725.205Persons who may report under this subpart.
§ 725.232Activities subject to the jurisdiction of other Federal programs or agencies.
§ 725.234Activities conducted inside a structure.
§ 725.235Conditions of exemption for activities conducted inside a structure.
§ 725.238Activities conducted outside a structure.
§ 725.239Use of specific microorganisms in activities conducted outside a structure.
§ 725.250Procedural requirements for the TERA.
§ 725.255Information to be included in the TERA.
§ 725.260Submission of health and environmental effects data.
§ 725.270EPA review of the TERA.
§ 725.288Revocation or modification of TERA approval.
§ 725.300Scope and purpose.
§ 725.305Persons who may apply under this subpart.
§ 725.350Procedural requirements for this subpart.
§ 725.355Information to be included in the TME application.
§ 725.370EPA review of the TME application.
§ 725.400Scope and purpose.
§ 725.420Recipient microorganisms.
§ 725.421Introduced genetic material.
§ 725.422Physical containment and control technologies.
§ 725.424Requirements for the Tier I exemption.
§ 725.426Applicability of the Tier I exemption.
§ 725.428Requirements for the Tier II exemption.
§ 725.450Procedural requirements for the Tier II exemption.
§ 725.455Information to be included in the Tier II exemption request.
§ 725.470EPA review of the Tier II exemption request.
§ 725.900Scope and purpose.
§ 725.910Persons excluded from reporting significant new uses.
§ 725.912Exemptions.
§ 725.920Exports and imports.
§ 725.950Additional recordkeeping requirements.
§ 725.975EPA approval of alternative control measures.
§ 725.980Expedited procedures for issuing significant new use rules for microorganisms subject to section 5(e) orders.
§ 725.984Modification or revocation of certain notification requirements.
§ 725.1000Scope.
§ 725.1075Burkholderia cepacia complex.
§ 725.1079Arsenic detecting strain of E. coli with extra-chromosomal elements, including an intergeneric screening marker (generic).
§ 725.1080Trichoderma reesei (generic).
§ 725.1081Trichoderma reesei modified (generic).
§ 725.1082Microorganism expressing enzymes (generic).