Course Description:
This course covers the theory of dissolution and compendial requirements for performing dissolution testing, including instrument qualification and verification testing. It also addresses reference materials and specifications for performance verification testing (PVT), with a focus on sources of variability in dissolution results.
The hands-on session of this training will start with the mechanical calibration of dissolution apparatus, followed by the PVT using the USP Prednisone Tablet and applying the PVT Calculation tool (GM and %CV). Finally, participants will perform the dissolution testing as per USP monograph and USP General Chapter<711> Dissolution.
Pricing varies. Please inquire for more info at https://go.usp.org/Services.
Upon completion of this course, you will be able to
- Explain the concept of dissolution testing and its instrumentation.
- Demonstrate good manufacturing practices when performing dissolution testing.
- Assess and identify variability that may affect dissolution testing results.
- Perform qualification of dissolution instrument including PVT and mechanical calibration.
Who should participate:
- National and private Pharmaceutical QC laboratories
- QA Manager
- QC Chemist
- QC Manager
- R&D