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Center for Biologics Evaluation and Research, U.S. Food and Drug AdministrationU.S. Food and Drug AdministrationCenter for Biologics Evaluation and Research
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FDA Home Page | CBER A-Z Index | CBER Search | Contact CBER | CBER Home Page

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CBER links to product areas
CBER links
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Consumer / Healthcare Information

Adverse Event Reporting
  - Biological Product Deviation Reporting
  - MedWatch
  - Transfusion / Donation Related Fatalities
  - Vaccine Adverse Event Reporting System

All About Vaccines for Kids

Clin Investigator Info

Counterfeit Initiative

Countering Bioterrorism

  - General
  - Blood
  - Vaccines

FDA Patient Safety News

Healthcare Letters

Keeping Blood Transfusions Safe

NIH Clinical Trials Database

NLM MEDLINEplus Health Information

Product Approvals

Product Labeling

Product Shortages

Recalls / Withdrawals

Safety Information

Vaccines Provide Effective Protection

Violative Advert / Promo Letters

Warning Letters
  - Other Compliance Actions

FDA Information
  - Consumers
  - Consumer Magazine
  - Health Professionals
  - Patients


CBER is responsible for ensuring the safety and efficacy of blood and blood products, vaccines, allergenics, and biological therapeutics. CBER's regulation of biological products has expanded in recent years to include a wide variety of new products such as biotechnology products, somatic cell therapy and gene therapy, and banked human tissues.

If you have questions or are unable to find the information you need, please contact:

Center for Biologics Evaluation and Research
Office of Communication, Training & Manufacturers Assistance
800-835-4709 or 301-827-1800


Transfer of Therapeutic Products to CDER


FDA Advances Consumer Health and Safety in 2003

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