This certification is designed for those working in a Medical Device Industry. Medical device industry is one of the rapidly growing industries in healthcare, driven by innovation and new technologies. The last few years have seen an unprecedented growth in innovative and improved technologies, which has led to the development of state-of-the-art medical devices and catalyzed growth and advancement in the healthcare industry. It is designed for professionals whose roles and responsibilities require that they understand the basics of Quality control and assurance as well as the points to be held while filing regulatory submissions. This programme gives maximum coverage of the foundations of the medical devices regulations and their application in the medical device market today and near future.
The case study based approach in certification programme is designed for working professionals in full time employment or those who have prior industry experience who want to update their knowledge and gain required skills and attitude in the area in order to become a certified professional in the domain. This certification is also beneficial for professionals from different streams to help them intensify their knowledge. This is an advanced certification having rigorous case studies based methodology throughout the duration.
Module 1: Introduction to Medical Devices
Module 2: Current Good Manufacturing Practices (India & International)
Module 3: Quality Management Systems and Risk Management to Medical Devices
Module 4: Regulations to Medical Devices (USA, EU and India)
Module 5: Bio compatibility Studies
Module 6: Clinical Trials for Medical Devices
Module 7: Overview of In-vitro Regulation and combination Products
Module 8: Medical Devices and Allied field
Graduate in any discipline is eligible for our Post Graduate Diploma and Certificate Programmes. For Executive Diploma programmes and Professional Certifications, you need to have at least 1 year of work experience.
Registrations are currently open for regular and online both modes.
A comprehensive study material for all the modules in hard copies ensuring the needs of the audience. The accompanying training material is appropriately aligned with the current Industry’s expectations.
All the participants are expected to appear for online assessment. After successful completion the participants will be certified as Medical Device Professional by IGMPI. For all the above mentioned elaborate study resources, Assessment test papers and case studies would be provided by the Institute from time to time. Details get updated on the webpage as well. The certification will be awarded after the required levels of knowledge, skills, professionalism and attitude are assessed through the IGMPI assessment process.
In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare like Dr. Reddy's Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, IPCA Laboratories, Calyx, Bliss GVS Pharma, SeQuent, Mankind, Beryl Drugs, Allergy Therapeutics, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy , Biocon etc. The IGMPI's Corporate Resource Division actively recommends our professionals 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 industries on regular basis.
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 to ensure design requirements incorporate the defined service strategy/serviceability, participating in design and program reviews to optimize implementation. Certified Medical Device Professional by IGMPI, open doors for entry into the industry which endows theoretical as well as practical knowledge to the candidate required to sustain successfully in industry. After the completion of this programme the candidate gets selected as Medical device Quality Assurance Manager, Regulatory Affairs Manager, Quality Assurance Compliance Specialist, Medical Devices Specialist etc.
S.No. | Programmes | Duration | Mode | Programmes Fee |
---|---|---|---|---|
1 | Certified Programmes | 3 months | Online | Rs.45,000/- (USD 700) |
For further enquiries, call or write to us on:
18001031071
(Toll Free -9:00 am to 5:30 pm IST-except on Central Government holidays)/
info@igmpi.ac.in
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