F. Regulatory and Clinical Development
Bioequivalence Study Fundamentals
Introduces the scientific and operational basis of bioavailability and bioequivalence studies for generic medicines.
Duration12 hours
Best ForRegulatory staff, pharmacists, clinical teams, R&D and graduates
FormatRecorded foundation \+ live workshop
Introduces the scientific and operational basis of bioavailability and bioequivalence studies for generic medicines. Topics include study design, reference product, pharmacokinetic parameters, ethics, bioanalysis, statistics, acceptance criteria and study reports.