ClinWorld’s Regulatory affairs team understands the importance of the highest quality regulatory submissions. We’ll work with you to Plan, Prepare & Complete global or local submissions and will Communicate, Interact and Liaise with regulatory agencies to ensure approval on time.
We Offer :
- To develop and present strategies and tactics needed to ensure regulatory compliance and maintain marketing authorizations.
- To prepare documents for IND, NDA, ANDA, CTD Submissions and also to support registrations of the new entities with MHRA, MCC, USFDA, TGA, Malaysia, European Union etc in concurrence with the regulations promulgated by a whole range of agencies like the Environmental Protection Agency, Federal Trade Commission, Occupational Safety & Health Administration and Drug Enforcement Administration.
- To utilize different approaches to latest regulatory practices through peer interactions.