Certificate Course in Drug Regulatory Affairs (DRA)
Duration: 3 Month(s)
Covalent Trainings
Hyderabad, Telangana, India
Course TypeCertificate
Course Specialty
Drug Regulatory Affairs
Overview
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.
Fee ():
-
Stipend (INR):
-
Accomodation:
As Per Availability
Scholarship:
-
Eligibility
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
Minimum Education
MBBSBAMS (Bachelor of Ayurvedic Medicine and Surgery)BHMS (Bachelor of Homeopathic Medicine and Surgery)DPharm (Diploma in Pharmacy)BSc (Bachelor of Science)BPharm (Bachelor Of Pharmacy)
Admission Process:
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)
