Cranfield University

Program Information

Format: Campus

Program Description:

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.

International Student Requirements:

Where applicable, students must achieve a minimum IELTS score of 6.5 or TOEFL 580. Our Academic English Summer Programme offers pre-sessional training in English.

Tuition & Financial Aid

Financial Aid Offered: No