Guideline

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21 CFR Part 312 Investigational New Drug Application
Short Title:	21 CFR Part 312
Internet:	http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=312&showFR=1
Origin/Publisher:	FDA
Content:	This part contains procedures governing the use of investigational new products including the submission to, and review by, the FDA.
Document Type:	Code of Federal Regulations