Recent advancements in BA/BE Research

The aim of bioavailability study is to find out the dosage form influence on the biological performance of the drug, sensitivity to detect differences in the rate and extent of absorption. Bioavailability and bioequivalence study design involves Single dose or multi dose standard 2x 2 crossovers, Parallel groups, for more than two formulations. A study design meant for estimating essential pharmacokinetic parameters differs significantly from a bioequivalence study meant for comparing the test formulation. The results of a pilot study can be used as the sole basis to document BA or BE provided the study’s design and execution are suitable and enough subjects have completed the study.

  • Novel Drug Delivery Systems- BA/BE approach
  • Generic drugs: Current claims and future directions
  • • BA/BE Studies for Immediate-Release Solid Oral Dosage Forms
  • Bioequivalence analysis of highly variable drugs
  • Bioavailability Study for cancer drugs
  • Food-effect bioavailability and fed bioequivalence studies

Related Conference of Recent advancements in BA/BE Research

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13th European Biosimilars Congress 2020

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May 18-19, 2020

30th Annual European Pharma Congress

Berlin, Germany
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cancer-research-2020

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6th World Congress on Medicinal Plants and Marine Drugs

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25th International Congress on Pharmaceutical Biotechnology

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12th World Congress on Neuropharmacology

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33rdWorld Congress on Pharmacology

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35th World Pharmacology and Toxicology Forum

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2nd World Congress on Drug Discovery and Drug Design

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Recent advancements in BA/BE Research Conference Speakers

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