Before a drug or a medical device can enter any market, it needs to fulfill all the applicable regulatory requirements and gain approval from the concerned regulatory bodies. Regulatory and demographic environment is a part of challenge to the pharmaceutical and the medical device industry. The real struggle is to define the strategy, development of appropriate business plan and efficient execution of the same. For that technical expertise is required. All employees should be aware of the expectations and procedures within the company. Assessment of employees is done on the basis of their knowledge and skill.
IGMPI offers Post Graduate diploma in Regulatory Affairs with the major area of thrust being the regulatory scenario for Medical Devices. The curriculum is designed and developed by experts from the medical device regulatory industry and is focused on both theoretical and practical aspects. The course is meant for Graduates and Post Graduates, employed plus yet to be employed candidates willing to enter this exciting field of liaison between the technical aspects of a medical device as well as the legal role of submissions and approvals.
IGMPI offers an opportunity for everyone to come and learn with us the intricacies of this exciting career choice and be a very good professional at it through the learning acquired here.
Module 1: Introduction to Global Regulatory Authorities for pharma and healthcare industries
Module 2: Medical Devices, In –vitro devices, Biologics & Combination Products: Introductory Module
Module 3: FDA Regulations and Guidelines on Medical Devices
Module 4: European Union Regulatory Guidelines on Medical Devices (Part 1 and Part 2)
Module 5: Medical Device Regulations from Indian perspective
Module 6: Management of the risks associated with Medical devices
Module 7: Biocompatibility Studies and Medical Devices
Module 8: Clinical Trials: Medical Devices
Module 9: Overview of In – Vitro Device Regulation
Module 10: Overview of Combination Products Regulation
Module 11: Medical Device Registration, e-Submissions and Approvals in US, Europe and India
Graduation in Pharma/Medical/Biomedical/Biotechnology/Microbiology/Science and Candidates appearing for the final year of Bachelor's degree/equivalent qualification exam or awaiting their results, are eligible to apply.
Minimum time in which a student can complete this diploma course is 12 months while a maximum of 24 months is allowed to complete the course.
The registration dates for this bi-annual programme run by the institute are updated timely on the webpage. The Training sessions and webinars are scheduled preferably on weekends depending on the availability of visiting faculty.. 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.
IGMPI follows a credit system based on all learning activities involved in studying for all PG Diploma, Executive Diploma and Certificate Programmes. Each of your modules is equal to 4 credits. To successfully complete the programme, you will have to earn all the credits assigned to your programme.
All the participants are expected to appear for an online exam and are also obliged to submit assignments after each module. After successful completion, the participants will be awarded Post Graduate Diploma in Regulatory Affairs (Medical Device as Major) by Faculty of Medical Device Management, IGMPI. For all the above mentioned modules elaborate course material, self-assessment assignments and project work details would be provided by the Institute from time to time. Details get updated on the webpage as well.
IGMPI offers placement assistance to its students. The Institute has partnered with many organizations for providing placement assistance to in its participants. Besides, it has a robust placement cell comprised of senior level Human Resources professionals and Talent Acquisition experts which maintains close links with business and industry. This cell is continuously engaged in promoting employability of our participants. The efforts of our placement cell also include helping with professional resume writing & interview skills. In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare, Medical devices 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, Biocon , Hindustan Syringes & Medical Devices, Wipro GE Healthcare, Medtronic, Bausch & Lomb, Baxter, Sushrut Surgicals, Wipro Technologies, HCL Technologies etc.
Medical Devices Industry is highly alluring sector now a days. Hence, there is fierce competition in this sector. Proper training and knowledge in this field is required so as to reach the pinnacle of success in this particular sector.
Professional and industry oriented training courses such as Medical Device Management by IGMPI, open doors for entry into the industry. Post Graduate Diploma in Regulatory Affairs (Medical Device as Major) is a broad spectrum course which endows theoretical as well as practical knowledge to the candidate required to sustain successfully in industry. After the completion of this course the candidate gets selected in industry/sector of his/her interest. This course is also beneficial for working professionals to gain hike in their sector by getting updated knowledge of the field.
Mr Vinod Arora, Principal Advisor, IGMPI
Placement testimonials: Our alumni are working with Fortune 500 and global Pharmaceutical, Food and healthcare giants like