Roundtable Discussion – Developing a Robust Characterization Assay Panel to Support GMP Release Assays and CQA Assessment

Time: 11:45 am
day: Conference Day Two


  • 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