Regulating Medical Devices – Wed 12 Feb

Understanding the roadmap to regulatory approval in different markets is an essential part of any business plan for a new medical technology. Developing the right regulatory strategy enables you to get your products to market quickly by achieving compliance with UK, EU and international standards. This course will equip you with a “how to” guide and covers all essential information you need to plan for your regulatory approval process.

For more information and to book for your place your place (free to NHS) Regulating Medical Devices – HTE