Introduction to Medical Devices

A comprehensive program covering all aspects of Medical Devices life cycle right from Global Regulatory Affairs, Quality Management Systems, Medical Devices Labeling, Post Market Surveillance. This basic program is suitable for individuals with no to minimum experience in medical devices industry. Led by industry leading Medical Devices Expert, this program is the right start for anyone who who wish to start their career in medical devices industry as Innovator, Engineer, Regulatory Professional, Marketing and Sales professional or entrepreneur. Our programs are backed by Real-Time project experience that provide a context to learning so participants can relate their knowledge to real-world problems in the medical devices indsut Chapters: 1- Introduction to Regulatory Affairs 2- Global Regulatory Bodies 3- Medical Device Value Chain 4- Regulatory Touch points across the Value Chain 5- Overview of QMS 6- Overview of Medical Devices Labelling 7- Overview of Global Regulatory Submissions 8- Overview of Post Market Surveillance 9- Real Time Regulatory Case Studies 10- Assignment for each topic