THIS WEBINAR WILL COVER:
How design and development activities are connected to your quality management documentation
Why you shouldn’t view your design controls as disconnected items
Why it’s important to document your design and development activities properly the first time
Why the belief that design and development documentation slows or hinders development is a myth
How the most progressive device companies are utilizing tools that enable clean trace matrices
The future state of these tools and how they’re trending toward becoming the industry standards
Q&A Session
WHO SHOULD ATTEND?
- Medical Device Executives
- Regulatory Affairs Professionals and Management
- Quality Professionals and Management
- Clinical Affairs Professionals and Management
- R&D Engineers and Management
Visit this webpage for details on this FREE webinar
https://www.greenlight.guru/webinar/avoiding-problems-design-risk-validation-documentation?
Event Information
Event Topic:
HOW TO AVOID COMMON PROBLEMS WITH YOUR DESIGN, RISK, AND VALIDATION DOCUMENTATION
Event Description:
https://www.greenlight.guru/webinar/avoiding-problems-design-risk-validation-documentation?
Date/Time:
Date(s) - 03/14/19
10:00 am - 11:15 am
Event Location:
Other: Internet Webinar
Event Details
Event Type
Webinar