40 CFR §725.424
Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
- (a)Conditions of exemption. The manufacture or import of a new microorganism for commercial purposes is not subject to review under this part if all of the following conditions are met for all activities involving the new microorganism:
- (1)The recipient microorganism is listed in and meets any requirements specified in § 725.420.
- (2)The introduced genetic material meets the criteria under § 725.421.
- (3)The physical containment and control technologies of any facility in which the microorganism will be manufactured, processed, or used meet the criteria under § 725.422.
- (4)The manufacturer or importer submits a certification described in paragraph (b) of this section to EPA at least 10 days before commencing initial manufacture or import of a new microorganism derived from a recipient microorganism listed in § 725.420.
- (5)The manufacturer or importer complies with the recordkeeping requirements of § 725.65 and maintains records for the initial and subsequent uses of the new microorganism that verify compliance with the following:
- (b)Certification. To be eligible for the Tier I exemption under this subpart, the manufacturer or importer must submit to EPA a document signed by a responsible company official containing the information listed in this paragraph.
- (1)Name and address of manufacturer or importer.
- (2)Date when manufacture or import is expected to begin.
- (3)The identification (genus, species) of the recipient microorganism listed in § 725.420 which is being used to create the new microorganism which will be used under the conditions of the Tier I exemption.
- (4)Certification of the following:
- (5)The site of waste disposal and the type of permits for disposal, the permit numbers and the institutions issuing the permits.
- (6)The certification statement required in § 725.25(b). Certification of submission of test data is not required for the Tier I exemption.