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
Learn more about our enterprise portal ->MDDplus: Cloud Computing for Medical Device Design
MDDplus provides access to medical
device design management tools from within the Salesforce Cloud. 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.
Now available for enterprise or Salesforce Cloud portals!!
