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.
|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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