Medical Device Courses In India

We offer a comprehensive range of medical device training courses covering a variety of formats including online public or if you prefer to have a group of employees attend a course together choose inhouse it s your choice.

Medical device courses in india.

Is the largest consumer of medical devices and leads the world in the production of medical devices. 78 e dated the 31st january 2017 are published and are mandatory with effect from 1st january 2018. We also offer a wide range of specialist courses. Executive diploma in medical device management is a fast track course which endows theoretical as well as practical knowledge to the candidate required to sustain successfully in industry.

Has a medical device market valued at more than 100 billion in 2008 roughly 42 percent of the world s total. These rules provided requirements for import manufacture clinical investigation medical device and in vitro diagnostics. We have the privilege of serving the health care industry in india for more than 32 years with world class medical devices in the diverse fields. Courses can be customised to your requirements.

Professional and industry oriented training courses such as medical device management by igmpi open doors for entry into the industry. Import and export of medical devices. Our expert tutors are industry leaders who have trained over 70 of the top 100 medical device companies globally so. To fill the regulatory vacuum in quality certification space for medical devices in the country the association of indian medical device industry aimed in collaboration with the quality council of india qci and the national accreditation board for certification bodies nabcb is rolling out a voluntary quality certification scheme for medical devices.

Online training in medical device regulation in india and worldwide. The course is meant for all those keen on being a part of medical device industry and even working professionals can apply for the course and affirm a strong position in the industry. Learn how to design and develop medical devices to international quality standards such as iso 13485 how to meet and keep ahead of medical device directive regulatory requirements and gain knowledge of the ce marking process. Recent amendments made in the rules by incorporating specific rules i e.

The course is ideal for usfda medical device regulation like 510k registeration pre market approval and labelling of medical device. The course is meant for graduates and post graduates employed plus yet to be employed candidates keen on taking medical devices industry as their career choice.