№ files_lp_4_process_3_113932
Guidance document outlining legally binding procedures for conducting and reviewing research involving recombinant or synthetic nucleic acid molecules, detailing regulatory responsibilities, approval processes, and biosafety requirements.
Year: 2026
Institution: National Institutes of Health (NIH)
Type of Document: Guidance / Regulatory Summary
Subject: Recombinant DNA (rDNA) and Synthetic DNA (sDNA) research
Author: NIH Office of Biotechnology Activities (OBA)
Target Audience: Researchers using NIH funds, Institutional Biosafety Committees
Scope: United States, applicable to institutions receiving NIH funding
Regulatory References: NIH Guidelines, CDC Select Agent Program, BMBL Manual
Compliance Requirements: Institutional Biosafety Committee (IBC) approval, RAC review, IRB approval for human research, adherence to biosafety and waste management protocols
Publication Date: 2026
Website Reference: http://osp.od.nih.gov/office-biotechnology-activities/biosafety/nih-guidelines
Price: 8 / 10 USD
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