MasterControl Registrations™ Toolkit for Medical Device Firms

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Videos 1 Toolkit MasterControl Registrations™ Toolkit for Medical Device Firms Registering products with the FDA in the United States or other regulatory bodies overseas is a key challenge for medical device companies. The challenge grows exponentially when companies manage multiple registration projects involving different markets across the globe. MasterControl prepared this toolkit to help address the difficulties most medtech firms experience during the product registration process. These free white papers, articles, and videos cover a wide range of topics—from effective management of dossier and device history files to FDA inspection tips and warning letter trends. MasterControl Registrations for Medical Device Firms This video gives you a tour of MasterControl Registrations, a robust product registration and submission management solution that will help launch your medical devices faster, better, and easier throughout the world. Transitioning from the Medical Device Directives to the new Medical Device Regulation The new European Medical Device Regulation (MDR) is in place. What does it mean for manufacturers? This free webinar explains what you need to do during the three-year transition period. Med Device Company Kerr Relies on MasterControl Kerr, located in Switzerland, has streamlined its regulatory processes and improved efficiency with the help of MasterControl. It manufactures Class I and II dental products.

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