Dissolution Testing, Equipment Requirements, Quality Control & Biowaivers
14 – 16 February 2022, live online training
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Summary
A unique online training course that integrates the in-vitro dissolution testing, equipment requirements, quality control aspects and using dissolution to obtain biowaivers.
Learning Objectives
- The role of dissolution studies and dissolution equipment
- Connecting the dissolution data to pharmacokinetics
- Quality control aspects of dissolution testing
- How to develop dissolution tests and how to interpret them
- About the requirements for studies in fasting and fed state
- How to obtain biowaivers with the use of dissolution studies
Key Topics
- Why do we need Dissolution?
- Development of dissolution tests
- Dissolution test equipment and its constraints
- QC aspects of dissolution testing
- Dissolution testing in stability testing
- Use of dissolution studies to obtain biowaivers
Who should attend?
Dissolution testing specialists, BA/BE managers, Pharmacokineticists, IVIVC scientists, Regulatory affairs managers, R&D scientists, QC and QA managers
Past participants
- Global Clinical Project Manager, Gedeon Richter
- Manager Clinical Affairs, Stada
- Head of Research and Development, Medichem
- IVIVC and AD Researcher, Lek – A Sandoz Company
- Analytical Development Scientist, Catalent
Our online training experience includes
- Our client zone – a single source for all training materials as well as pre and post-training communication
- Live interactive format via the Zoom platform
- Direct interaction with the trainer
- Q&As, case studies, polls
- Revisit recorded sessions for 30 days
- Training in digital format
- Digital and LinkedIn certificates