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About CBER FAQs
Does CBER conduct inspections?
How are biological products approved?
How do biological products differ from conventional drugs?
How do I find out about ongoing clinical trials to treat AIDS or Cancer?
How do I get a copy of the Code of Federal Regulations that pertain to regulation of biological products?
How do I or my doctor report an adverse event to FDA?
What are the advantages to the public for regulation of biologics under the PHS Act?
What does "CBER" stand for?
What is a biological product?
What is CBER's response to public health threats and bioterrorism?
What is CBER's role after a biological product is approved and in use?
What is the Center for Biologics Evaluation and Research (CBER)?
What is the contact information for CBER's Manufacturers Assistance Branch?
What is the legal authority for regulating biological products?
What products does CBER regulate?
Last revised: March 30, 2007
