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Vintara ISO 13485 -- Setting the Standard in Regulatory Compliance
Vintara’s Enterprise Portal helps leaders deploy world class best practices for the manufacture and sale of medical devices. Our configurable workflow applications will drive performance and world class regulatory compliance including:. 21 CFR Part 11 compliance. 21 CFR Part 820 compliance. Learn more about our enterprise portal -. MDDplus: Cloud Computing for Medical Device Design. Now available for enterprise or Salesforce Cloud portals!
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ISO 13485 certification providers in Delhi Mumbai Bangalore Kolkata Pune Chennai India
Medical Device Quality Management System (ISO 13485:2016). Worldwide recognised ISO 13485 Certification services. ISO 13485 is the most widely used for medical devices throughout the world. We offers best ISO 13485 Certification in all cities, India. Reduces trade barrier to enter into international market such as Europen Market. ISO 13485 certification help medical device manufacturer to meet requirement of European Medical Device Directives. What is ISO 13485? Why to get ISO 13485? How to get ISO 13485?
