E. Dennis Bashaw

fda drug development clinical pharmacology clinical trials orphan drugs rare disease fda sunscreen regulatory absorption dermal drug development bioanalytical methods validation bioavailabilty aaps drug policy regulations nonprescription drugs food and drug administration must rulemaking maximal usage healthcare science toxicology risk management phase 1 first in human personalized medicine dermatology konect bioequivalence gastrointestinal drugs china 2016