This course provides an opportunity that on-the-job learning doesn't. By attending this course, you will gain a basic understanding of the European medical device regulatory requirements and how to comply with them.
When & Where?
12 November 2020
Standard Fee: £360.00 plus 23% VAT
- Regulatory affairs professionals who require a comprehensive overview of medical devices
- Who work in functions allied to medical device regulatory affairs (such as marketing, medical, quality, packaging and legal)
- Those who work in regulatory authorities and those in the regulatory sector