The United States Department of Agriculture (USDA), Animal and Plant Health Inspection Service (APHIS), Biotechnology Regulatory Services (BRS) welcomes you to the
In September 2007, APHIS–BRS introduced the Biotechnology Quality Management System (BQMS) Program as a voluntary program to help the regulated community develop sound quality management practices regarding the importation, interstate movement, and environmental release of genetically engineered (GE) organisms that are, or may be, plant pests, as described in our regulations at 7 CFR part 340. The Program was an all or nothing, recognized, quality management system which over time became too costly and burdensome for small and academic organizations.
APHIS BRS reexamined the Biotechnology Quality Management System Program after engaging with current and prospective participants, and determined that a modularized web-based approach will reach a wider universe of researchers and developers conducting biotechnology activities under APHIS regulations at 7 CFR part 340.
APHIS published a Federal Register notice in early 2017 announcing this new Biotechnology Quality Management Support Program, renaming it from the Biotechnology Quality Management System Program, but retaining the “BQMS” acronym.
The new BQMS Program remains a voluntary compliance assistance program to facilitate compliance with APHIS’ biotechnology regulations, and provides compliance assistance information and education in a more flexible and adaptable way.
For the BQMS modules, see the BQMS Program User Orientation Webpage.
For other BQMS Informational Materials, see the BQMS Informational Materials Webpage.
Still have questions, comments or suggestions? Contact us via email: BRS.BQMS@aphis.usda.gov
Disclaimer: This material is provided as a generalized guide for your organization’s quality management practices relevant to your obligations under APHIS regulations found at 7 CFR part 340. Use of these modules and its content does not guarantee that the user’s activities are in compliance with 7 CFR part 340, and it does not eliminate the user’s obligations under any other statute or regulation. If your organization wishes to use formal quality management systems, it is best to rely on qualified quality management professionals.