Medical Technology Regulatory Affairs

Start: Throughout the year

Duration: 2-5 years PT

Course Details:

For many years, the production and marketing of pharmacologically active drugs has been highly regulated and controlled. Until recently, however, the medical devices industry was subject to far less regulation. Now, following the implementation of several EU directives and national legislation, professionals concerned with the regulation of medical devices will have to adopt and adapt to significantly more rigid working practices.

This course provides a detailed insight into current and proposed legislation in the area and education in the processes and practices required for its implementation. It is accredited by TOPRA, The Organisation for Professionals in Regulatory Affairs.

Entry Requirements:

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.

English language requirements - Our normal minimum requirement is a TOEFL score of 580 (paper test) or 237 (computer test), essay rating 4.5 or 92 (Internet test), all skills 19 or an IELTS 6.5 with 6.0 for writing, a TOEIC overall score of 830, or a Cambridge Certificate of Proficiency in English grade C or Cambridge Certificate in Advanced English grade C, although a number of our programmes require higher scores.

Funding:

For details of any scholarships and bursaries, contact enquiries@cranfield.ac.uk or +44(0)1234 758008 for further information.

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