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Center for Devices and Radiological Health / Office of Regulatory Affairs / Center for Biologics Evaluation and Research / Title 21 of the Code of Federal Regulations / Center for Drug Evaluation and Research / Regulatory affairs / Medical device / Biologic / Good Clinical Data Management Practice / Food and Drug Administration / Medicine / Health
Center for Devices and Radiological Health
Office of Regulatory Affairs
Center for Biologics Evaluation and Research
Title 21 of the Code of Federal Regulations
Center for Drug Evaluation and Research
Regulatory affairs
Medical device
Biologic
Good Clinical Data Management Practice
Food and Drug Administration
Medicine
Health

Staff Manual Guide[removed]

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