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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


Staff Manual Guide[removed]
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Company

DEMO/AMB / /

Organization

FDA / office of Communication / office of Medical Products and Tobacco / Center for Devices and Radiological Health / office of Compliance / office of Operations / office of Global Regulatory Operations and Policy / office of Regulatory Affairs / Center for Drug Evaluation / office of Medical Products / office of Device Evaluation / office of Communication and Education / /

Person

Margaret A. Hamburg / /

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Position

Deputy Associate Commissioner for Regulatory Affairs / Director and Deputy Director / Associate Commissioner for Regulatory Affairs / Director / Commissioner / Director and Deputy Director / Center / Commissioner of Food and / /

Technology

In Vitro Diagnostics / /

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