The number refers to several distinct official documents, regulations, and technical materials. Depending on your specific interest, here are the primary "312" guides: 1. Security: Standard Form 312 (SF-312)
Sponsors must submit an IND to the FDA before starting a clinical investigation. The number refers to several distinct official documents,
You agree never to divulge classified information unless the recipient is authorized by the USG to receive it. 2. Pharma: 21 CFR Part 312 (IND Applications) The number refers to several distinct official documents,
This FDA regulation governs . It provides the legal framework for clinical trials on human subjects. The number refers to several distinct official documents,
Investigators must supervise the administration of the drug and ensure it is only given to authorized subjects.