An IND is submitted to the FDA following the successful completion of Phase 3 clinical trials.
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Q21: In recent years,screening out drugs that may
Q22: In 2008,the U.S.Pharmacopeia identified double the number
Q23: Without a doubt,FDA-approved drugs are safe.
Q24: OTC drugs,by definition,do not have any side
Q25: The length of time that a patent
Q27: A drug patent has a fixed duration
Q28: The FDA estimates that over a period
Q29: The FDA approval process can be shortened
Q30: Bioequivalence refers to two drug compounds having
Q31: As a result of the Kafauver-Harris Amendment
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