(510k) Format and Contents for Various Device Types Including In Vitro Diagnostic Devices
Federal Statutes and Regulations Governing Medical Devices in the US
Who should Attend
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)
Past Events
An Interactive Workshop on Premarket [510(k)] Notification Submissions 2012 - 01 Nov 2012, Grand Hyatt San Francisco, California, United States (33756)
Important
Please, check "An Interactive Workshop on Premarket [510(k)] Notification Submissions" official website for possible changes, before making any traveling arrangements
