Basic info
Industry
software development
Sectors
Authorizations
ISO 13485
Quality management systems
21 CFR Part 820
820.30 – Design Controls
Users
Controlling design and development
Ensuring compliance
History versions
Health Care
Compliance with regulatory requirements
Advanced Gantt
21 CFR Part 11
Start-ups to large companies).
Consulting
Saving expenses and time
Documents
Arranging
Software
Medical device
Information Technology
Tool
Date founded
2015