January 26, 2016

InstantGMP™ MD



InstantGMP™ MD is a cloud based Electronic Device History software that is compliant 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.

InstantGMP™ MD Features

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
  • Are you expanding? InstantGMP™ MD can accommodate several users at once time! Be sure to inquire about pricing, users are sold by 5-user basis

InstantGMP™ MD Features