Points of Consideration during Medical Device Design and Development - Dos and Donts 2014
28 Oct 2014
Webinar
Description
Topics
Device Design Concept
Statutes and Regulations
Design and Development Planning
Definitions
Design Control System Components
Key Considerations
Design Input and Design Output
Design Control Sub-Systems
Design V and/or V
Design Review
Design History File (DHF), Device History Record (DHR) and Device Master Record (DMR)
Design Transfer and Design Changes
How to Prepare for FDA inspection for Design Control
Common Mistakes and How to Avoid
Speaker`s Recommendation and Suggestions on PASS-IT Solutions
Best Practices based on Actual Cases
Who should Attend
Quality professionals (associates, specialists, managers, directors or VPs)
Regulatory affairs (associates, specialists, managers, directors or VPs)
Complaint and risk management personnel
R&D (engineers, scientists, managers, directors or VPs)
Contractors/subcontractors
Consultants
VPs
CEOs
Clinical affairs (associates, specialists, managers, directors or VPs)
Past Events
Points of Consideration during Medical Device Design and Development - Dos and Donts 2014 - 28 Oct 2014, Webinar (47539)
Important
Please, check "Points of Consideration during Medical Device Design and Development - Dos and Donts" official website for possible changes, before making any traveling arrangements
