Medical Technology Regulatory Affairs
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.
1st or 2nd Class UK Honours degree, or equivalent, in a science, business or management subject, normally with at least 2 years experience in an appropriate working environment.
|Qualification||Study mode||Start month||Fee||Course duration|
|Campus name||Town||Postcode||Region||Main campus||Campus||Partner|
|Cranfield Campus||Milton Keynes||MK43 0AL||South East|
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