Title 40 -- Protection of Environment

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PART 725 -- REPORTING REQUIREMENTS AND REVIEW PROCESSES FOR MICROORGANISMS

   
Subpart A -- General Provisions and Applicability

      §725.1 Scope and purpose.
      §725.3 Definitions.
      §725.8 Coverage of this part.
      §725.12 Identification of microorganisms for Inventory and other listing purposes.
      §725.15 Determining applicability when microorganism identity or use is confidential or uncertain.
      §725.17 Consultation with EPA.
   
Subpart B -- Administrative Procedures

      §725.20 Scope and purpose.
      §725.25 General administrative requirements.
      §725.27 Submissions.
      §725.28 Notice that submission is not required.
      §725.29 EPA acknowledgement of receipt of submission.
      §725.32 Errors in the submission.
      §725.33 Incomplete submissions.
      §725.36 New information.
      §725.40 Notice in the Federal Register.
      §725.50 EPA review.
      §725.54 Suspension of the review period.
      §725.56 Extension of the review period.
      §725.60 Withdrawal of submission by the submitter.
      §725.65 Recordkeeping.
      §725.67 Applications to exempt new microorganisms from this part.
      §725.70 Compliance.
      §725.75 Inspections.
   
Subpart C -- Confidentiality and Public Access to Information

      §725.80 General provisions for confidentiality claims.
      §725.85 Microorganism identity.
      §725.88 Uses of a microorganism.
      §725.92 Data from health and safety studies of microorganisms.
      §725.94 Substantiation requirements.
      §725.95 Public file.
   
Subpart D -- Microbial Commercial Activities Notification Requirements

      §725.100 Scope and purpose.
      §725.105 Persons who must report.
      §725.110 Persons not subject to this subpart.
      §725.150 Procedural requirements for this subpart.
      §725.155 Information to be included in the MCAN.
      §725.160 Submission of health and environmental effects data.
      §725.170 EPA review of the MCAN.
      §725.190 Notice of commencement of manufacture or import.
   
Subpart E -- Exemptions for Research and Development Activities

      §725.200 Scope and purpose.
      §725.205 Persons who may report under this subpart.
      §725.232 Activities subject to the jurisdiction of other Federal programs or agencies.
      §725.234 Activities conducted inside a structure.
      §725.235 Conditions of exemption for activities conducted inside a structure.
      §725.238 Activities conducted outside a structure.
      §725.239 Use of specific microorganisms in activities conducted outside a structure.
      §725.250 Procedural requirements for the TERA.
      §725.255 Information to be included in the TERA.
      §725.260 Submission of health and environmental effects data.
      §725.270 EPA review of the TERA.
      §725.288 Revocation or modification of TERA approval.
   
Subpart F -- Exemptions for Test Marketing

      §725.300 Scope and purpose.
      §725.305 Persons who may apply under this subpart.
      §725.350 Procedural requirements for this subpart.
      §725.355 Information to be included in the TME application.
      §725.370 EPA review of the TME application.
   
Subpart G -- General Exemptions for New Microorganisms

      §725.400 Scope and purpose.
      §725.420 Recipient microorganisms.
      §725.421 Introduced genetic material.
      §725.422 Physical containment and control technologies.
      §725.424 Requirements for the Tier I exemption.
      §725.426 Applicability of the Tier I exemption.
      §725.428 Requirements for the Tier II exemption.
      §725.450 Procedural requirements for the Tier II exemption.
      §725.455 Information to be included in the Tier II exemption request.
      §725.470 EPA review of the Tier II exemption request.
   
Subpart L -- Additional Procedures for Reporting on Significant New Uses of Microorganisms

      §725.900 Scope and purpose.
      §725.910 Persons excluded from reporting significant new uses.
      §725.912 Exemptions.
      §725.920 Exports and imports.
      §725.950 Additional recordkeeping requirements.
      §725.975 EPA approval of alternative control measures.
      §725.980 Expedited procedures for issuing significant new use rules for microorganisms subject to section 5(e) orders.
      §725.984 Modification or revocation of certain notification requirements.
   
Subpart M -- Significant New Uses for Specific Microorganisms

      §725.1000 Scope.
      §725.1075 Burkholderia cepacia complex.