Global Medical Device Regulations - US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan 2012

Global Medical Device Regulations is a seminar dedicated to medical device regulations of twelve (12) countries concerning medical devices, active implantable medical devices and in vitro diagnostic medical devices for adequate implementation and successful registration..

Global Medical Device Regulations brings together:

• Quality assurance, quality control, and quality systems (associates, specialists, engineers, managers, directors and VPs)
• Regulatory affairs (associates, specialists, managers, and directors)
• Product and development (associates, scientists, managers, directors and VPs)
• Research and development (associates, scientists, managers, directors and VPs)
• Site managers, and consultants
• Contract research organization (associates, scientists, managers, directors and VPs)
• Contractors and subcontractors
• Senior and executive management (VPs, SVPs, Presidents and CEOs)