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Regulatory Affairs Branch (RAB)
RAB Main
Model Agreements
NCI - Cooperative Group - Industry Relationship Guidelines
Intellectual Property Option Policy
FDA Sites
Databases of Marketed Drugs
IND Application Process
Code of Federal Regulations
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Organization Chart
CTEP Branches
and Offices
Office of the
Associate Director
Clinical Grants and Contracts Branch
Clinical Investigations Branch
Clinical Trials Monitoring Branch
Investigational
Drug Branch
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Regulatory Affairs Branch
Administrative Resource Center
Last Updated:
10/08/08
Code of Federal Regulations
Title 21
Part 50: Protection of Human Subjects
Part 56: Institutional Review Boards
Part 58: GLP's
Parts 210-211: GMP's
Part 312: INDs
Part 314: Approval Applications
Part 600 : Biological Products