Dr Gerd Michael Maier, Boehringer Ingelheim
In the pharmaceutical industry, drug dissolution testing is routinely used as a key test parameter for assessing the performance of solid and semi-solid dosage forms in both drug development and quality control. A dissolution test measures the amount of drug that goes into solution over a period of time under standardized conditions. It is used to assure batch-to-batch quality, to provide process control, and to substitute in vivo studies under certain circumstances.
This webinar targets executives and staff in development and quality control in the pharmaceutical industry. The webinar is also intended for participants from quality assurance, regulatory affairs as well as contract laboratories.
To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.
Timing and Duration:
When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.
In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.
Training Course Documentation and Certificate:
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.
This webinar aims at providing delegates with a sound understanding of the principles and practices in dissolution testing.
The following topics will be covered:
- Dissolution technique
- Factors affecting dissolution
- Regulatory requirements (general guidelines, USP, EP)
- Dissolution methods and apparatus
- Dissolution automation
- Qualification of dissolution apparatuses
- Development of dissolution methods
Recording from 04.09.2020
Duration of recording: about 1.5 h.