NLM Digital Collections

Search

Search Constraints

Start Over You searched for: Subjects United States. Department of Health and Human Services Remove constraint Subjects: United States. Department of Health and Human Services

Search Results

211. Initiation of voluntary recalls under 21 CFR Part 7, subpart C: guidance for industry and FDA staff

213. Master protocols: efficient clinical trial design strategies to expedite development of oncology drugs and biologics

216. Providing regulatory submissions in electronic and non-electronic format: promotional labeling and advertising materials for human prescription drugs

219. Facet screw systems: performance criteria for safety and performance based pathway : guidance for industry and Food and Drug Administration staff

220. Denture base resins: performance criteria for safety and performance based pathway : guidance for industry and Food and Drug Administration Staff