An IND is submitted to the FDA following the successful completion of Phase 3 clinical trials.
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Q4: There is a greater quantity of available
Q4: If a medication is eventually going to
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
Q10: The Dietary supplements are the most regulated
Q11: A drug patent has a fixed duration
Q12: Phase 4 trials occur after a drug
Q13: Establishing an LD50 for a new drug
Q14: Phase 2 trials are typically conducted on
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