The root cause of variable or inconsistent data from compendial dissolution tests can be difficult to identify. Formulation, equipment, operator error and incorrect calculation may be factors. This webinar presents a systematic, logical approach to investigating anomalous dissolution results.
Why Should You Attend:
Pharmaceutical dissolution testing for solid oral dosage forms is a complex analytical procedure where the control of critical variables (environmental conditions, equipment performance, sample introduction, sampling and dissolution medium preparation) is important for achieving consistent results. With so many factors at play, assigning root cause to anomalous data can be difficult.
By attending this webinar, you will learn how to approach dissolution OOS/OOT investigations in a systematic, rigorous manner.
The benefits of attending this webinar include:
Areas Covered in the Webinar:
Who Will Benefit: