Medical Device Regulatory Affairs Training
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It discusses how iso13485 2003 the iso standard relates to the industry of medical devices details the regulatory ex.
Medical device regulatory affairs training. Medical device development and fda meetings. We have dynamic course owners around the world allowing delivery of training in many local languages. Online courses for industry on safety and effectiveness of medical devices and exposure to radiation from medical devices. This course will provide a basic comprehensive overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
The regulatory function is vital in making safe and effective healthcare products available worldwide. The regulatory affairs certificate. Orau free online courses for state local and tribal regulatory partners. Essentials of european medical device regulatory affairs.
You will have six months to complete all nine courses of the program. Learn more or enroll in our rac gracp certification course here. Online training in regulatory affairs for medical devices. 22 2020 nov.
Medical devices is achieved by completing four core and five elective courses. Learn about the medical device regulatory affairs and ra qa training courses offered in 12 us cities by oriel stat a matrix. This global medical device regulatory affairs professional certification program is an online program which guides the student through a global medical device regulations overview. 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.
Essentials of european pharmaceutical regulatory affairs. 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. 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. The office of regulatory affairs and quality is pleased to offer the regulatory affairs training program.
The program is 6 weeks and consists of weekly online lectures combined with independent study. This program is open to all interested individuals who register.
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