The Generic Drugs Advisory Committee is to advise on the safety and effectiveness of human generic drug products for use in treating "a broad spectrum of human diseases." The Drug Abuse Advisory Committee, with a broad charge, advises the FDA Commissioner on "the scientific and medical evaluation of all information The Food and Drug Administration regulates more than 150,000 marketed drugs and medical devices. At any time, nearly 3,000 investigational new drugs are being developed. More dietary supplements than ever before are on the market, and Americans today have a much broader range of food choices. Then there are the scores of blood products and veterinary medicines for which the FDA is responsible.
• Institutional Review
Board (Independent review).
• Withdrawals.
• End point justification
of clinical trial phases.
• Phase repetition.
• Data Integrity and archival.
Other types of committees in Hospital
1. Infection Control
Committee.
2. Central sterile supply
Committee.
3. Biodegradable waste
committee.
4. Medical Record Committee.