Free Seminar Day “From validation to release testing – a strategical view on practical aspects of validation, dissolution and CCIT”
You work in the pharmaceutical industry and you are interested in modern methods and tasks around in the pharmaceutical industry? Then we are looking forward to welcoming you to our one-day seminar in Hamburg on 16th of May 2024.
Ensuring the validation of biopharmaceutical methods within a Good Manufacturing Practice (GMP) environment is critical for regulatory compliance and patient safety. This seminar will offer real-world case studies and insights which highlight effective strategies for conducting ICHQ2 R2 method validation in a Quality Control (QC) setting.
Attendees will gain practical knowledge and valuable insights into the challenges, best practices, and regulatory considerations of performing validations and transfers within a GMP QC environment.
Here you will get an overview of our highly informative agenda.
Furthermore, get ready to elevate your understanding of GMP quality control dissolution and CCIT challenges through case studies and insightful discussions, unlocking a world of opportunities in optimizing pharmaceutical quality and patient well-being.
Moderators:
Speakers:
- Jennifer Borrelli – ICHQ2 R2 Validation of Analytical Procedures – Changes and Impact
- Kristian Groetzinger – Standards and practical insights on the transfer of pharmaceutical analytical methods under GMP
- Alexis Guillot – In vitro drug release testing: From theory to praxis, a key to overcome dissolution challenges
- Xiao Yu Xie – Dissolution: a major role in drug product development & quality control
- Luca Pietro Carati – Container Closure Integrity Testing (CCIT) in the drug products lifecycle
After the presentation we will host a guided tour through our services laboratories in Hamburg.
In all lectures, a lively and open discussion and questions on your part are expressly desired.
Date and location:
Date: 16th of May 2024 from 9.00am - 5.00pm
Location: Am Neuländer Gewerbepark 1, 21079 Hamburg, Eurofins BioPharma Product Testing, Meeting-Room „John Nash“
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