This course provides an opportunity that on-the-job learning doesn't: network and learn from a variety of experts including your fellow delegates. 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?
16 October 2019 09:30-16:30
Course fee for delegates £360.00 plus 20% 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)
- From related professions (law, pharmaceutical manufacturing, marketing and sales, healthcare, administration, project management)
- Those who work in regulatory authorities and those in the regulatory sector