Post Graduate Diploma in Regulatory Affairs. The PG Diploma in regulatory affairs envisages the whole regulatory aspect as it helps the participants to imbibe the necessary knowledge which will make them a specialized person of the field to independently deal with the regulatory aspects of a food company.
After successful completion, the participants will be awarded Post Graduate Diploma in Pharmaceutical Regulatory Affairs by Faculty of Good Manufacturing Practice, IGMPI. For all the above mentioned modules elaborate course material and project work details would be provided by the Institute from time to time.
Batches. The objective of Post Graduate Diploma in Drug Regulatory Affairs program is to develop students, over the period of 6 months, by in depth industry oriented knowledge to reach top end positions in the pharmaceutical regulatory affairs industries. This program is developed and structured in a manner to match high academic standards and …
Postgraduate Diploma Regulatory Affairs (Medical Devices) – Eight modules in total, this requires at least six modules from B and you can choose up to two modules from A (120 credits in total). Postgraduate Certificate – requires the completion of any four modules from A or.
Post Graduate Diploma in Drug Regulatory Affairs is a Diploma level Pharmacy programme. The course helps to provide a comprehensive education in the important aspects of Regulatory and Quality Compliance in the pharmaceutical industry. Students are encouraged to enhance their knowledge of regulatory and compliance issues and to explore careers …
location_on Campus-2:- Near Lok Manya Tilak, Janta Inter College, Meerut Road, Morta Police Chowki, Ghaziabad, Uttar Pradesh. call (0120) 2835119 / phone_iphone 9810177860, 9310835119, 8800201631. Courses Offered. Post Graduate Diploma in Drug Regulatory Affairs . Post Graduate Diploma in Geriatric Medicine.
Regulatory Affairs course aims at entry to middle level industry professionals. As DRA is an ever growing and dynamic field continuous learning and knowledge updating is the key to survival. The course is developed to provide in depth knowledge about pharmaceutical regulatory affairs .
