Discussing Optimal Documentation Curation & Management for Efficient Creation & Reproducibility of Your QC Testing to Enhance Development Processes & Regulatory Compliance for Your mRNA Therapeutics

Time: 1:31 pm
day: Pre-Conference Day


As we navigate the intricacies of developing and producing mRNA-based treatments, the accuracy, accessibility, and compliance of our documentation play a pivotal role in ensuring regulatory adherence, reproducibility, and ultimately, the efficacy of our therapeutic interventions. Join us as we delve into the strategies, best practices, and

innovative approaches to curate and manage documentation effectively, providing you

with the tools to optimize your mRNA therapeutic development journey.

Join this session to discuss:

  • What is the critical role documentation plays in the development and production of mRNA therapeutics
  • What are the different categories of documentation in mRNA therapeutics
  • What is the significance of traceability and standardization documentation procedures