Intelligent Automation
Customized AI Engines and ISO 18587 Certification for Medical Device Labeling Translation
AI Engines Trained with +30 years of Medical Device Content and Implemented According to ISO 18587 to Help Meet the Increased Content Requirements of MDR and IVDR
Device manufacturers are discovering that the MDR and IVDR have created a “content tsunami” – and the only way to keep up is through automation. In order to address the avalanche of MDR/IVDR labeling and labeling-like content (SSCPs, SSPs, surgical techniques, etc), manufacturers are turning to TransPerfect’s customized AI-supported process to help cut the cost and turnaround of translation, without sacrificing quality.
Intelligent Automation for MDR & IVDR Content: Summary of Safety & Clinical Performance (SSCP), Summary of Performance (SSP), and Selected Labeling
Content requirements under the EU’s MDR and IVDR, including the translation of labeling, marketing, SSCPs, SSPs, and clinical communications, are set to dramatically increase. Currently, most device manufacturers use manual processes and document-based applications like Microsoft Word and InDesign to manage their content. However, manual processes and document-based approaches require additional headcount to handle increased volumes and faster turnarounds. Intelligent automation is the right solution.
