Conducting & Managing Bioequivalence & Bioavailability Studies

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Conducting & Managing Bioequivalence & Bioavailability Studies

pharmaceutical business analytics distance course

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✔ ACCRE USA Accredited
✔ Program developed by senior industry experts
✔ eBooks – Presentation & Notes on Cliniminds LMS
✔ Cliniminds Certification after completion of program
✔ MCQ based final exams
✔ Pharmacokinetics Basics | Bioavailability & Bioequivalence: Regulatory Terminology | Regulatory Aspects of BE Studies | Need for Bioequivalence Studies: NCEs & Generic Drugs | Intellectual Property Rights & TRIPs Agreement | Generic Drugs, ANDA Approval, Reference List of Drugs & Orange Book | Approaches to Bioequivalence Studies | Types of BA/BE Studies | Design & Conduct of Bioequivalence Studies | Study Personnel & Their Role | Facilities for BA/BE Studies (CRO Checklist) | Clinical, Bio-Analytical, & Quality Assurance Departments | Managing BE Studies | Measurement Methodology | Analysis of BE Studies | Food Effect BE Studies | Biowaivers

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