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

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Presentation transcript:

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)

InstantGMP Material Screen InstantGMP ensures materials are in compliance with SOPs

Specifications and Version Control

InstantGMP Inventory Use Screen

InstantGMP Project Screens

InstantGMP Design History File Management

InstantGMP Design Master Record Tabs

InstantGMP Device Master Record Manufacturing Instructions

InstantGMP Device History Record Instructions Screen

Tracking of Inventory Distribution

InstantGMP Reports

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