Bioequivalence study

July 16, 2015

The European Medicines Agency (EMA) has released for consultation a document relating to productspecific guidance on bioequivalence studies for four active substances - asenapine, prasugrel, sitagliptin and zonisamide. EMA says it’s decided to routinely publish product-specific bioequivalence guidance to provide a more consistent apporach to the assessment of marketing authorisation applications for generic medicines in the EU.

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Pharmacy DailyPharmacy Daily | Bioequivalence study

Bioequivalence study

Other recent headlines

Prescribing endorsement consultation opens

Call for embedded rural pharmacist pilot

MTick: Behind the menopause ‘one-stop shop’

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES