Postgraduate degree in Chemistry from a recognized University/Institution Or MPharm with Pharmaceutical Chemistry from a recognized University / Institution
Materiovigilance Programme of India, Indian Pharmacopoeia Commission IPC, an Autonomous organization under the Ministry of Health and Family Welfare. Masters in Clinical Pharmacology / Regulatory Science. Good knowledge of computers and experience in Medical Device Industry
Degree in Pharmacy or Pharmaceutical Sciences or Medicine with specialization in Clinical Pharmacology or Microbiology or equivalent from a recognized University
BACHELOR OF PHARMACY, BACHELOR OF SCIENCE (B.Sc Degree ), MASTER OF PHARMACY, MASTER OF SCIENCE. Understanding of safety regulatory report documents in terms of purpose of the different sections, data flow and applicable regulations.
Master Degree (M. Pharma/M.S.) in Pharmaceutics / Pharmacology / Pharmaceutical Chemistry / Pharmacognosy / Pharmaceutical Technology Research experience in formulation development of herbal drugs.
Post Graduate Degree from a recognized University / Institute in Biotechnology / Molecular Biology / Pharmaceutical biotechnology / Pharmaceutical Analysis /or equivalent