Simple, Compliant Document Management for Medical Device Companies
CMD’s web-based document control system is built for medical device companies that need 21 CFR Part 11 compliance without the complexity or cost of traditional solutions.
Simple by design.
No lengthy implementation | No complex training | Works from day 1
What Makes Our System Different
Simple
Ready to use on Day 1. No lengthy implementation, no complex training.
Affordable
Reasonably priced for small companies and startups. Similar tools cost $40k+ per year.
Compliant
Designed for 21 CFR Part 11 compliance from the ground up.
Proven
Built by the quality experts at CMD MedTech. Field-tested by CMD and our customers.
How We Use It
For Our Own QMS
CMD MedTech uses the system internally to manage all documents under our ISO 13485:2016 certified Quality Management System.
For Customer QMS
We offer our electronic document control system as part of our Quality Management System services. Software licensing and support are included in the service package.
Key Features
- Web-based platform with secure, customer-specific portals
- Electronic document review and approval
- Continuous backup of all electronic records
- Validation and maintenance included
- Updated regularly for current regulations and standards