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Technology / Medical device / Center for Devices and Radiological Health / Title 21 of the Code of Federal Regulations / Design controls / Sousan S. Altaie / Medicine / Food and Drug Administration / Health


Overview of the FDA Submission Process Nina Hunter, PhD FDA/CDRH/OIR/DIHD NCI SBIR Workshop on Federal Resources to
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Document Date: 2013-06-04 15:39:56


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Company

In Vitro Diagnostics / /

IndustryTerm

collection devices / manufacturing / diagnostic products / diagnostic algorithms / /

MedicalCondition

allergy / tumor / cancer / disease / infectious disease / /

Organization

FDA / Immunology and Hematology Devices Division of Microbiology Devices Division of Radiological Health Division / Mammography Quality Standards Office / Chemistry and Toxicology Devices Division of Immunology / Science and Engineering Laboratories office of Surveillance and Biometrics / Regulatory Authority / office of Medical Products and Tobacco / Center for Devices and Radiological Health / Division of Chemistry / Center for Drug Evaluation / Center for Tobacco Products / Compliance office of Device Evaluation / office of Science / /

Person

Nina Hunter / /

Position

Director / /

PublishedMedium

Microbiology / /

URL

http /

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