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Our new article outlines best practices for navigating an uncertain regulatory environment for mRNA-based products, and explores why partnering with a contract development and manufacturing organization (CDMO) can provide biotechnology and pharmaceutical companies with peace of mind when it comes to adhering to regulatory guidelines.
Specifically, the article covers the following topics:
- Current and developing regulatory guidance for mRNA products
- The importance of early engagement with regulatory bodies
- Choosing a strategic CDMO partner for mRNA development