Roundtable Discussion – Developing a Robust Characterization Assay Panel to Support GMP Release Assays and CQA Assessment
Time: 11:45 am
day: Conference Day Two
Details:
- Discussing the requirements of a strong characterization assay panel
- Defining GMP standards in relation to LNP Drug Products
- Overviewing CQA criteria with an understanding of the assays available to clearly present the data with an appreciation of the gaps in the industry as it stands
