Medical Device 2012 - 2-day In-person Seminar: Medical Device Quality Systems, CAPA and European Medical Device regulations

ISO 13485:2003 is a quality management system standard specially written for the medical device industry and is on the U S Food & Drug Administration (FDA) list of recognized consensus standards. ISO 13485 is also a critical system to assist with compliance to Canadian Medical Device regulations, European Medical Device (MDD) and IVD Directives, Japanese PAL requirements, and many other international regulatory requirements. Who will Benefit

This seminar will benefit medical device companies interested in understanding and implementing a quality management system that is universally accepted by regulatory authorities.

Employees who will benefit include:
- Quality & Regulatory Professionals
- Quality System Auditors
- Manufacturing & Design Engineers
- Marketing Product Managers