Regulatory Affairs Industrial Training

Service Description

Regulatory Affaires Will include following Topics 1. Preparation and Submission of New drug Application and Abbreviated New drug 2. Application for various Regulatory bodies e.g. UDFDA, EU, TGA etc. 3. Preparation of Master batch Records 4. Clinical Trails Phases (Phase-I, II and III) 5. Drug Master File Preparation 6. Drug Dossier Preparation 7. Other activities associated with Regulatory Affaires