Medical Devices 2012 - Anticipated Changes to the EU Medical Device Directives; 2012 Changes and What the Future Holds for Licensees

This Medical Device Directive training will discuss the recently implemented and currently planned changes to the Medical Device Directives across the EU.

Why Should You Attend:

This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.

Who Will Benefit:

This workshop will be of great value to Medical Device professionals and those involved in the registration of Medical Devices across the EU. It is primarily designed to benefit the following disciplines:

- Clinical research and medical operations

- Project Managers

- Product Development personnel

- Manufacturing personnel

- Researchers managing Medical Device R&D and Development

- Quality Assurance such as GMP, GCP Auditors

- Regulatory affairs

- Clinical trial supply personnel

- CRO personnel

- All personnel who need to understand the procedures and impact of placing Medical Devices on the Market across the EU