Special Considerations during Medical Device Design: Dos and Don`ts 2014 is a webinar that covers topics such as:
- 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
Special Considerations during Medical Device Design: Dos and Don`ts 2014 is intended for:
- 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
- Other interested parties
- Clinical affairs (associates, specialists, managers, directors or VPs)