InstantGMP™ MD

InstantGMP™ MD Quality System Software

Medical Device Manufacturing

Our software, InstantGMP™ MD, is an all-in-one Quality Management System (QMS) software that connects a Quality Assurance, Documents, and cGMP Inventory Management with Device History Records. Designed by Quality and Regulatory experts, each module is seamlessly linked to help companies with the complexities of regulations, 510k submissions, and much more. InstantGMP™ MD comes pre-validated to meet the requirements for Part 11, GAMP 5, the FDA standards for computer system validation, and ISO 13485. With our software, your company can benefit from improved product quality and consistency, compliance, and traceability with streamlined and automated workflows. Want to take advantage of the Internet of Things (IoT)? Customization and Integration services are available to help you tailor the software to your company's unique needs. Companies can also take advantage of the Medical Device Standard Operating Procedures (SOPs) set that comes with the software within the Document Management System (DMS).

 

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