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| Name | Medical Device Regulation Training - MDSAP Training |
| Video Uploader | Video From NSF |
| Upload Date | This Video Uploaded At 24-09-2018 19:40:38 |
| Video Discription | Click here to view the MDSAP courses: https://nsf.learnupon.com/store NSF International launches eLearning training that covers global medical device regulatory requirements for all five countries participating in the Medical Device Single Audit Program (MDSAP). The training modules offer a comprehensive overview of each country's medical device regulatory framework, including both premarket and post-market requirements, an introduction to MDSAP and how each country utilizes MDSAP. Throughout each course, students will be reminded of the additions to the MDSAP audit model for that particular country. Competency assessments provide documented evidence for the training requirements of ISO 13485:2016, the international quality management system standard for medical devices. The modules include: Medical device regulatory requirements for Australia Medical device regulatory requirements for Brazil Medical device regulatory requirements for Canada Medical device regulatory requirements for Japan Medical device regulatory requirements for the U.S. For additional information please call us at 1 202 822 1850. 9S5v0283UzY |
| Category | Education |
| Tags | MDSAP | ISO 13485:2016 | elearning | NSF medical devices | Medical Devices | Medical device regulation | Kim Trautman | Heather Howell | Medical device development | FDA regulations | EU MDR | regulation training | Regulatory training | NSF International | NSF Medical Device | Medtechcon |
