Taught course

Medical Technology Regulatory Affairs

Institution
Cranfield University · Cranfield University
Qualifications
MScPGDipPGCert

Entry requirements

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

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.

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

MSc

part time
24-60 months

PGDip

part time
24-48 months

PGCert

part time
36 months

Assessment

AssessmentWhat kind of work will I be doing? (proportionally)
Written/ formal examinations20
Written coursework / continuous assessment30
Dissertation50 (20000 words)

Course contact details

Name
Enquiries Office
Email
enquiries@cranfield.ac.uk
Phone
+44 (0)1234 758008