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Regulatory Affairs Industrial Training

Providing Classes on Regulatory affairs

  • 1 hour
  • Online

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

Upcoming Sessions

Contact Details


Computer system Validation (CSV ) training and certification, Sector D, Sudama Nagar, Indore, Madhya Pradesh, India

Service Page: Bookings_Service_Page
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