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Course content

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!

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