21 cfr 312 subpart h

21 cfr 312 subpart h

21 CFR Part 211, Subpart H - Holding and Distribution. Status message. There are 3 Updates appearing in the Federal Register for 21 CFR Part 211.
Such systems found expression in FDA's promulgation in 1988 of the IND Subpart E regulation (21 C.F.R. Part 312) and in 1992 of the NDA Subpart H regulation.
Subpart B--Investigational New Drug Application (IND) · § Subpart D-- Responsibilities of Sponsors and Investigators Subpart H [Reserved]. Subpart. United States Code U. The Food and Drug Administration FDA is amending its regulations governing drug establishment registration and drug listing. This website has been translated to Spanish from English, and is updated. Subpart B-Investigational New Drug Application IND. Instructions for Downloading Viewers and Players. Federal Rules of Civil Procedure. Quick Links: Skip to main page content. 21 cfr 312 subpart h TPEP Symposium - Examining Challenges in Tissue Availability & Rapid Deployment (Session B)