Meryem Chennan

Company: CureVacSE

Job title: Senior Manager Regulatory Affairs CMC

Seminars:

Roundtable Discussion: How to Create a Reference Document to Facilitate Smooth Approval of mRNA Therapeutics in Compliance with Industry Regulations 12:00 pm

Delving into how to give evidence of a state of control and maintain regulatory compliance for your mRNA analytical techniques Unveiling strategies to incorporate innovative mRNA analytical technologies in alignment with GMP guidelines Understanding the process of standardizing mRNA analytical techniques to conform to CQAs and CPIs, thereby enabling efficient and expeditious approvalRead more

day: Conference Day One