January 26, 2016

InstantGMP™ MD

InstantGMP™ MD Quality System Software

InstantGMP™ MD is a cloud based Electronic Device History Quality System software for GMP compliance that is built-in with Part 820 and the production requirements of ISO 13485. The software guides users through the work flows required for manufacturing medical device products of all classes. It is pre-validated to comply with Part 11, GAMP 5 and the FDA requirements for computer validation. Customization and Integration services are available.

Some of the features of InstantGMP™ MD:

  • Improves the quality and consistency of your medical device manufacturing
  • Electronically keeps track of all of your Device Master Records and Device History Records
  • Establishes traceability in the event of a recall
  • Reduces the complexity of manufacturing batches of medical devices
  • Keeps specifications organized with version control
  • Copies existing master records or lets you make adjustments with ease
  • Updates inventory levels in real time
  • Scales batches with the click of a button for quick response to customer orders
  • Recalculates material quantities automatically on Bill of Materials and in manufacturing instructions
  • Turn-key Quality System

InstantGMP™ MD Features