What Device Firms Should Know about Design Control for an Adequate Implementation 2015
05 May 2015
Webinar
Key Topics
Introduction and Definitions
Federal Statutes and Regulations Governing Medical Devices in the US
Design Input
Design and Development Planning
Design Review
Design Output
Design Transfer
Design Verification And Validation including Software Validation
Design History File (DHF)
Design Changes
Device Master Record (DMR)
Device History Record (DHR)
Speaker’s PASS-IT recommendations/suggestions
Enforcement Actions
Who should Attend
Regulatory Affairs
R&D Scientists, Engineers, Managers, and Directors
Product Development Professionals
Quality Professionals
Consultants
CROs
Contractors and Subcontractors
Senior Management
Past Events
What Device Firms Should Know about Design Control for an Adequate Implementation 2015 - 05 May 2015, Webinar (51491)
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Important
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