Medical Device Regulatory Affairs Training

Medical devices is achieved by completing four core and five elective courses. Individuals who ensure regulatory compliance and prepare submissions as well as those whose main job function is clinical affairs or quality assurance are all considered regulatory professionals. This program is open to all interested individuals who register.

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Essentials of european pharmaceutical regulatory affairs.

Medical device regulatory affairs training.

Learn more about regulatory. It discusses how iso13485 2003 the iso standard relates to the industry of medical devices details the regulatory ex. Online courses for industry on safety and effectiveness of medical devices and exposure to radiation from medical devices. The program is 6 weeks and consists of weekly online lectures combined with independent study.

Orau free online courses for state local and tribal regulatory partners. Cfpie s regulatory affairs training and certification program was designed by industry experts to offer a comprehensive study of regulatory principals pitfalls and guidelines provided by governmental organizations. The office of regulatory affairs and quality is pleased to offer the regulatory affairs training program. You will have six months to complete all nine courses of the program.

This course will provide a basic comprehensive overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment. 19 2020 live and on demand online training. Essentials of european medical device regulatory affairs. Online training in regulatory affairs for medical devices.

22 2020 nov. This global medical device regulatory affairs professional certification program is an online program which guides the student through a global medical device regulations overview. Medical device development and fda meetings. Learn about the medical device regulatory affairs and ra qa training courses offered in 12 us cities by oriel stat a matrix.

The regulatory function is vital in making safe and effective healthcare products available worldwide. We have dynamic course owners around the world allowing delivery of training in many local languages. The regulatory affairs certificate. Design and develop medical devices to international quality standards ensure smooth submission meet iso 13485 standards satisfy customers and keep ahead of all regulatory developments with our medical devices training courses.

After successfully completing all nine courses you will receive a certificate recognizing your achievement. Learn more or enroll in our rac gracp certification course here.

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