Medical Device Regulatory Affairs Training Courses

Medical device regulatory training 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.

Medical device regulatory affairs training courses.

The one day courses are for very new recruits pas administrators and support staff in regulatory affairs and other related areas such as medical manufacturing and marketing. Medical devices training nsf international provides regulatory and quality medical devices training courses and professional qualifications. Our course library is monitored constantly to ensure that offerings stay up to date with evolving and changing requirements. Fda s office of regulatory affairs ora offers free high quality web based training for state local and tribal.

Nsf s training courses are highly interactive and based on real scenarios helping you meet international requirements throughout the product lifecycle. Introduction to medical device recalls. Online courses for industry on safety and effectiveness of medical devices and exposure to radiation from medical devices. You will have six months to complete all nine courses of the program.

After successfully completing all nine courses you will receive a certificate recognizing your achievement. Basics of regulatory affairs we offer one day basics courses in pharmaceutical veterinary and medical device regulatory affairs. Overview this master of science in medical device regulatory affairs presents students with the opportunity to skills to employers and peers and to enhance your career in regulatory affairs by developing increasing levels of competence and professionalism. Put together by practising medical device regulatory affairs professionals this newly researched and updated course is demanded by regulatory affairs managers who wish to get their people up to speed on current european medical device regulatory practices.

The regulatory affairs certificate. Medical devices is achieved by completing four core and five elective courses. No one knows better than you what your regulatory learning needs are so who better to build a certificate program that meets them. It is the gold standard in the field.

Medical device regulatory affairs ra qa training courses medical device ra qa training we offer basic through advanced courses in quality assurance regulatory compliance and accredited training for auditor development.