1. InstantGMP MD/PRO Electronic Device History File Software for Manufacturing Medical Devices in compliance with 21 CFR Part 820 (Quality System Regulation) and Part 11 (Electronic Documentation)

3. InstantGMP Material Screen InstantGMP ensures materials are in compliance with SOPs

4. Specifications and Version Control

6. InstantGMP Inventory Use Screen

7. InstantGMP Project Screens

8. InstantGMP Design History File Management

9. InstantGMP Design Master Record Tabs

10. InstantGMP Device Master Record Manufacturing Instructions

11. InstantGMP Device History Record Instructions Screen

12. Tracking of Inventory Distribution

13. InstantGMP Reports