In today’s digitized world, the continuous innovation of the newest product designs and development have uplifted the supremacy of the medical device manufacturing segment. However, specific regulations around it have resulted in reasonable administrative tasks and enhanced legal certainty of the global medical device system. Since medical device regulations are continually evolving alongside technological advancements, manufacturers must embrace data management procedures that help with ongoing compliance and regulations. This online medical device program has been developed for those who are involved with ensuring regulatory compliance for medical devices and industry veterans who need extra training on these topics and to clear basic concepts.
Course 1
Introduction and General Concept of Medical Device
Course 2
International Medical Device Regulation Practices
Any graduates pursuing in the field of Pharmaceutical Sciences, Medical Sciences, Veterinary Sciences, Biotechnology, Microbiology and Life Sciences from any recognized institution.
INR 40000/- per Year for Indian Nationals
USD 600 per Year ( Equivalent in INR would be charged)
My objective is to work ethically towards the betterment of Pharmacy Profession and contribute young nurtured students for a better India.
Dr M P Gowrav is presently working as Assistant Controller of Examinations and assistant professor in the Department of Pharmaceutics.
He is having 11 years of research experience and about 12 years of teaching experience, he has published 80 scientific papers in peer reviewed national and international journals.
He has guided 27 PG students and presently guiding 05 PG students.
He is member of various professional national organizations.
He is presently guiding 04 PhD research scholars.
He has recieved ICMR grant for 30.17 lakhs.
He has served as a NSS Programme Officer of the college from 2015-2022. He was a part of the organizing committee of National Integration Camp in 2016, 2018 & 2020. He has recieved a appreciation award as Contingent leader from Government of Karnataka for organizing NIC.
He was the coordinator of M.Pharm Pharmaceutical Regulatory Affairs from 2021-2022.
He is also currently serving as knowledge partner for Biocon Academy for Global research program which is joint intiative of BIocon and JSSAHER.
He has authored 03 book chapters.
3D Printing in Healthcare, Multiparticulate Drug Delivery Systems, Regulatory Science