The effectiveness of pharmaceutical dosage forms relies on the drug dissolving in the fluids of the gastrointestinal tract prior to absorption into the systemic circulation. The rate of dissolution of the product is therefore crucial.
To achieve reliable and reproducible results, it is important that analysts understand the importance of correctly setting up and sampling from the chosen apparatus.
Who should attend?
This 2 day course is designed for professionals new to dissolution testing and those with previous experience seeking to improve their skills and knowledge, working in the following areas
- Analytical Development
- Project Management
- Quality Control
- Quality Assurance
- Regulatory Affairs
- Pharmaceutical Development
For further information and online registration visit our website