CFR /  Title 40  /  Part 725: Reporting Requirements And Review Processes For Microorganisms

Section No.	Description
Section 725.1	Definitions
Section 725.3	Coverage of this part
Section 725.8	Identification of microorganisms for Inventory and other listing purposes
Section 725.12	Determining applicability when microorganism identity or use is confidential or uncertain
Section 725.15	Consultation with EPA
Section 725.17	Scope and purpose
Section 725.20	General administrative requirements
Section 725.25	Submissions
Section 725.27	Notice that submission is not required
Section 725.28	EPA acknowledgement of receipt of submission
Section 725.29	Errors in the submission
Section 725.32	Incomplete submissions
Section 725.33	New information
Section 725.36	Notice in the Federal Register
Section 725.40	EPA review
Section 725.50	Suspension of the review period
Section 725.54	Extension of the review period
Section 725.56	Withdrawal of submission by the submitter
Section 725.60	Recordkeeping
Section 725.65	Applications to exempt new microorganisms from this part
Section 725.67	Compliance
Section 725.70	Inspections
Section 725.75	General provisions for confidentiality claims
Section 725.80	Microorganism identity
Section 725.85	Uses of a microorganism
Section 725.88	Data from health and safety studies of microorganisms
Section 725.92	Substantiation requirements
Section 725.94	Public file
Section 725.95	Scope and purpose
Section 725.100	Persons who must report
Section 725.105	Persons not subject to this subpart
Section 725.110	Procedural requirements for this subpart
Section 725.150	Information to be included in the MCAN
Section 725.155	Submission of health and environmental effects data
Section 725.160	EPA review of the MCAN
Section 725.170	Notice of commencement of manufacture or import
Section 725.190	Scope and purpose
Section 725.200	Persons who may report under this subpart
Section 725.205	Activities subject to the jurisdiction of other Federal programs or agencies
Section 725.232	Activities conducted inside a structure
Section 725.234	Conditions of exemption for activities conducted inside a structure
Section 725.235	Activities conducted outside a structure
Section 725.238	Use of specific microorganisms in activities conducted outside a structure
Section 725.239	Procedural requirements for the TERA
Section 725.250	Information to be included in the TERA
Section 725.255	Submission of health and environmental effects data
Section 725.260	EPA review of the TERA
Section 725.270	Revocation or modification of TERA approval
Section 725.288	Scope and purpose
Section 725.300	Persons who may apply under this subpart
Section 725.305	Procedural requirements for this subpart
Section 725.350	Information to be included in the TME application
Section 725.355	EPA review of the TME application
Section 725.370	Scope and purpose
Section 725.400	Recipient microorganisms
Section 725.420	Introduced genetic material
Section 725.421	Physical containment and control technologies
Section 725.422	Requirements for the Tier I exemption
Section 725.424	Applicability of the Tier I exemption
Section 725.426	Requirements for the Tier II exemption
Section 725.428	Procedural requirements for the Tier II exemption
Section 725.450	Information to be included in the Tier II exemption request
Section 725.455	EPA review of the Tier II exemption request
Section 725.470	Scope and purpose
Section 725.900	Persons excluded from reporting significant new uses
Section 725.910	Exemptions
Section 725.912	Exports and imports
Section 725.920	Additional recordkeeping requirements
Section 725.950	EPA approval of alternative control measures
Section 725.975	Expedited procedures for issuing significant new use rules for microorganisms subject to section 5(e) orders
Section 725.980	Modification or revocation of certain notification requirements
Section 725.984	Scope
Section 725.1000	Burkholderia cepacia complex
Section 725.1075	Scope and applicability