ISO 13485

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:

  • ISO 13485
  • 21 CFR Part 11 compliance
  • 21 CFR Part 820 compliance
  • CAPA
  • Device Master Records
  • Customer Complaints
  • Nonconformances

MDDplus: Cloud Computing for Medical Device Design

The MDDplus application ensures that management and design teams can access, respond to, and administer design changes within a SaaS application. Vintara's MDDplus cloud application provides medical device medical design teams with the tools for managing a seamless design process from inception through delivery.