Bioequivalence: Intersection Between Science & Regulatory
Wednesday, Nov 5 8:30a
Westin San Diego
Carmel Valley,
CA
In order for generic drugs to be approved, the FDA requires bioequivalence studies to make sure the generic drug, when administered will have the same effect as the branded drug. However, ensuring the drug's safety can be a very complex and costly process with a high failure rate. A challenge that often creates a bottleneck between the scientific community and regulatory agencies. What can be done to bridge the gap between scientific community and the regulatory agencies in safely bringing a new… Show more
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Location & Nearby Info
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