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CERTIFICATE PROGRAMME IN  DRUG REGISTRATION (INDIA)

This course provides integrated knowledge and broad perspectives required to effectively manage the regulatory process for approval of new drugs in India. This course targets all Pharma manufacturer/importer, regulatory, preclinical, formulation scientists, and clinical trial professional who are involved directly or indirectly in new drug registration process. The course modules covers new drug including fixed-dose combination in India. Ever-changing laws and regulations require regulatory affairs professionals to cater the current needs of industries for the global competition so as to effectively bring their medicinal products to the Indian market with less time.

Module 1 :Regulatory Overview in India and Regulatory Dossier

Module 2 :Registration of Drug in India

Eligibility

Any Life Science graduate/ B.Pharm/M pharm/MSc/Phd in science disciplines/ any diploma holder or passed outs of Clinical Research degree or diploma courses are eligible for these course. Working professionals of any of the following industry types Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology or any related industry are highly encouraged to apply for the programme.

Programme Duration

The candidate is expected to complete the course in a minimum of 1 and maximum of 3 months.

Registration

The registration dates for this programme run by the institute are updated timely on the webpage. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self regulated and self-paced performance to the participants.

Programmes Fees

A one-time fees (lump sum paid at beginning of the course) of Rs 7,500/- (300 USD for oversees students) is mandatory. This covers for the course registration fees, tuition fees, course material examination fee etc.

Examination & Certification

All the participants are expected to appear for online exam and are also obliged to submit assignments after each module. After successful completion the participants will be awarded Certificate in Drug Registration (India). For all the above mentioned modules elaborate course material, assignment and case studies would be provided by the Institute from time to time. Details get updated on the webpage as well.

Corporate Relations

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy's Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, IPCA Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy , Biocon etc. The IGMPI's Corporate Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare and Food industries on regular basis.

Future career prospects

The objective of these courses is to impart knowledge and practical understanding about the drug registration procedures that are available and the structure of the registration dossier. Professionals who are willing to have a successful career in regulatory affairs, registration and documentation for European Countries, GCC Countries, India, US market should attend this course. These courses are highly recommended for those who are aspiring to move into regulatory affairs from other areas within a pharmaceutical company.

How to apply

For further enquiries or Prospectus, write to or call us on:
[email protected]/+91 8587838177, +91 8130924488, 0120-2427175, 0120-4375280