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Content Automation for Medical Device Manufacturers
Learn How Major Device Makers Cut Costs and Turnaround Times with TransPerfect’s CCMS Technology
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.
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