Over the past several months, the FDA has been planning for and making updates to its eMDR submission process. These changes have the potential to interrupt your submissions process if your complaint handling solution isn't ready.

From a quality perspective, complaints represent the most damaging defects - those that have reached a customer. Complaints also pose tough compliance challenges in terms of accurate determination and timely regulatory reporting. 

In this on-demand webinar, we'll present solutions for ensuring compliance and improving quality by automating complaint handling and eMDR submissions. We'll also focus on recent FDA updates that can affect your organization's ability to submit if you're not prepared. 

Watch this webinar to learn how Pilgrim's best practice complaint handling workflows and updated regulatory submission capabilities:

  • Improve complaint-related data integrity
  • Prioritize complaints for investigation
  • Determine global regulatory reporting needs
  • Ensure uninterrupted eMDR submissions
  • Drive continuous improvement and reduce cost of poor quality 

Download this on-demand webinar to learn more. »

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