The main aim of the Bio Equivalence and Bio Availability-2019 is to
promote the regulations related to Bio Equivalence and Bio
Availability were put into place, considering the latest advances in
the science. A significant role in the discovery, development, and
regulation of new drug products involves in recent research of Bio
Equivalence and Bio Availability. a crucial component of abbreviated
new drug applications (ANDAs), leading to market access of safe,
effective, and low cost in the advance studies of bioequivalence.
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20/08/2019 Last update