Medical Devices 2012 - Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs

This Medical device training will be discussing 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.

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 in the EU (25 expanded countries)