The Pure Food and Drug Act of 1906 guaranteed that drugs were useful and safe as long as ingredients were clearly labeled.
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Q1: After the passage of the 1938 Food,Drug,and
Q3: The result of the Kefauver-Harris Amendment of
Q4: If a medication is eventually going to
Q4: There is a greater quantity of available
Q5: Bioequivalence refers to two drug compounds having
Q6: Prior to 1906,drugs did not have to
Q7: Phase 2 trials utilize a double-blind placebo
Q9: An IND is submitted to the FDA
Q10: The Dietary supplements are the most regulated
Q11: A drug patent has a fixed duration
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