Certificate Course in Drug Regulatory Affairs (DRA)

Freshers or final-year students in life sciences, pharma, or health sciences

Good written English and basic understanding of drug development

Passion for regulatory documentation and compliance

The Regulatory Affairs (Entry Level) course at Covalent Trainings provides essential knowledge about the regulatory frameworks governing pharmaceutical products across global markets. Students learn about ICH guidelines, CTD/eCTD dossier compilation, submission procedures, and regulatory documentation for agencies like USFDA, EMA, and CDSCO. This job-oriented program prepares candidates for entry-level roles such as Regulatory Affairs Associate or Executive in pharmaceutical companies.

Contact Covalent Trainings (via phone/email/website)

Fill in the registration or inquiry form

Receive course brochure, fee structure, and batch dates

Pay fees and confirm batch slot

Attend sessions (online/offline depending on your preference)