Who Should Attend:
- Complaint Handling Units
- Regulatory Affairs Professionals
- TrackWise business owners and administrators
What You Will Learn:
Medical Device and Diagnostics organizations are faced with increased e-reporting expectations but what does it really mean? Hear the latest on eMDR and eMDV with strategies for compliance in a changing environment while also maintaining process capabilities to support the regions that are still paper based.
This webinar will also walk through the options for compliance for eMDR and review both the manual Webtrader and automated EDI scenarios. Attendees will be given tools to help them determine the business benefits of implementing the ‘high volume’ EDI option as well as understand the extra steps needed to deploy the ‘low volume’ Webtrader option so that informed decisions can be made at each firm as they evaluate compliance options.
Lastly, we’ll review a typical implementation of the high volume EDI solution in TrackWise and share lessons-learned from previous implementations.