CMC Services Regulatory Affairs Specialist  

Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. […]
Write and review of CTD Module 3.2.P Drug Product for new Marketing Authorizations, variations and renewals and for Clinical Trials Applications (CTAs). Support Clients in answering to Regulatory Authorities Deficiency Letters. […]
Guarantee that Patheon Monza site manufacturing processes and testing are performed...