1st or 2nd class UK Honours degree, or equivalent, in a science, business or management subject, preferably with experience in a relevant role within the healthcare industry.
Months of entry
January, December, November, October, September, August, July, June, May, April, March, February
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.
Fees and funding
Places on this course are usually self-funded or sponsored by the student's company. Please note that a formal offer of a place on this course must have been received before consideration can be given for funding.
Qualification and course duration
|Assessment||What kind of work will I be doing? (proportionally)|
|Written/ formal examinations||20|
|Written coursework / continuous assessment||30|
|Dissertation||50 (20000 words)|
Course contact details
- +44 (0) 1234 758540