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Medical Technology Regulatory Affairs (MSc/PgDip/PgCert)


Course Description

Regulatory affairs professionals play an important part in coordinating scientific endeavour with regulatory demands throughout the life of a medical device product from design conception through manufacture to market.
This part-time executive course provides professionals working in medical device regulatory affairs with a recognised way of formalising your skills, whilst retaining in employment with the flexibility to fit around your current job and responsibilities.

Visit the Medical Technology Regulatory Affairs (MSc/PgDip/PgCert) page on the Cranfield University website for more details!

Entry Requirements

A first or second class UK Honours degree, or an equivalent, in a science, business or management subject, preferably with two years’ experience in a relevant role within the healthcare industry. In certain cases a blend of qualifications, motivation and relevant experience will be acceptable. Available on a part-time basis only the course is specifically designed for industry professionals working within regulatory affairs who would like to train to further their careers.

Last Updated

14 July 2017

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Recipient: Cranfield University

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