cGMPs for Medical Devices, Including In Vitro Diagnostic Devices 2012
26 Jun 2012
Webinar
Key Topics
Definitions
QSRs for medical devices and in vitro diagnostic devices
Quality system (QS) requirements
Flexibility of the QSRs
Audits
Management responsibility and personnel
Design history file (DHF)
Design control: design and development planning, design input, design output, design review, design verification, design validation, design transfer, and design changes
Quality system procedures
Device master record (DMR)
Who should Attend
Regulatory affairs (associates, specialists, managers, and directors)
Manufacturing professionals
Quality assurance, quality control, and quality systems (associates, specialists, engineers, managers, directors and VPs)
Clinical affairs (associates, specialists, coordinators, managers, directors and VPs)
Product and development (associates, scientists, managers, directors and VPs)
Research and development (associates, scientists, managers, directors and VPs)
Contract manufacturing organization (associates, scientists, managers, directors and VPs)
Site managers, and consultants
Senior and executive management (VPs, SVPs, Presidents and CEOs)
Contract research organization (associates, scientists, managers, directors and VPs)
Contractors and subcontractors
Past Events
cGMPs for Medical Devices, Including In Vitro Diagnostic Devices 2012 - 26 Jun 2012, Webinar (30798)
cGMPs for Medical Devices, Including In Vitro Diagnostic Devices 2026
Important
Please, check "cGMPs for Medical Devices, Including In Vitro Diagnostic Devices" official website for possible changes, before making any traveling arrangements
