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Bioavailability and Bioequivalence
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This 2 day intensive seminar will equip you with a comprehensive overview and tools for effective BA/BE studies:
- Understand the essential components to achieve Therapeutic Equivalence in early pharmaceutical design
- Gather key insights into application of Pharmaceutic principles and Pharmacokinetic parameters for successful Bioequivalence studies
- Implement practical tips to help you understand In Vivo-In Vitro Correlation (IVIVC) for BE studies
- Conduct latest Good Clinical Practices in BE studies
- Apply Pharmaceutical equivalence in product development to meet BE and regulatory requirements
- Assess troubleshooting concepts when product is Bioinequivalence
Who Should Attend
- Research & Development
- Product / Business Development
- Formulations
- Product life-cycle development/management
- Strategic Planning and Alliances of Generic Manufacturing
- Regulatory Affairs & Product Compliance
- Technical Service & Manufacturing
- Quality Assurance & Quality Control
Seminar Led by:
Associate Professor Dr Azizi Ayob
(MD, PhD), Corporate Technical Advisor
PT Dexa Medica Group, Indonesia
Dr Azizi has over 15 years’ experience as a lecturer, researcher, head of technical and consultant in drug research and development (R&D), clinical pharmacology, pharmaceutical sciences and biopharmaceutical technology.
Appointed as Associate Professor of Pharmacology, winning various scientific awards and best PhD thesis since 2000, he was the Chief Scientific Officer and Consultant Pharmacologist at the Pharmaceutical R&D Centre of Chemical Company of Malaysia (CCM), involved in projects in early stage formulation, analytical and bioequivalence studies. In his current role, he is responsible for managing the pharmaceutical R&D and Regulatory Affairs teams.
