Fill out the form to watch the full 30-min panel discussion

Content Automation for Medical Device Manufacturers

Learn How Major Device Makers Cut Costs and Turnaround Times with TransPerfect’s CCMS Technology

background image
Webinar cover image

New Math for MDR/IVDR Content & Updates

It’s no secret that the MDR and IVDR include new content requirements – including labeling revisions, new types of documentation (e.g. SSCP, SSP), and more frequent updates. Now, device makers are discovering the complexity of maintaining accurate regulatory content across multiple documents – where a single change in 150 documents across 23 languages = 3,450 discreet changes to implement, QC, and republish. Learn how device makers like Carestream and Medtronic have addressed this challenge with TransPerfect’s CCMS content automation technology.

  • _

  • _

  • _