Panel Discussion: Reviewing Standards & Regulatory Requirements of the Analytical Field of mRNA-Based Therapeutics
Time: 8:45 am
day: Day Two
Details:
- Delving into how to give evidence of a state of control and maintain regulatory compliance for your mRNA analytical techniques
- Revealing how to integrate the new novel mRNA analytical technologies to align to GMP guidelines
- Understanding how to standardize your mRNA analytical techniques to align to CQAs and CPIs to allow efficient and rapid approval
