Regulatory
About Us
Cerbios has almost thirty years of experience and knowledge in successfully submitting DMFs for APIs and HPAIs to the major authorities worldwide.
Type II DMFs to the US FDA , DMF or CEP to regulatory authorities in Europe and translated DMFs to the Japanese PMDA through Cerbios’s agent are common practice and a service available for our biotech partners that need this expertise in-house with no need for additional consultants.
