Get to Know InstantGMP™ MD
All-in-one manufacturing & quality software for medical device producers.
We provide cloud-based Electronic Device History Record software with integrated modules that manage documents, inventory, and quality assurance together with the device history records. The software will guide you through the workflows required for manufacturing medical device Class II and Class III products. It is pre-validated to comply with Part 11, GAMP 5, the FDA requirements for computer validation, and lays the foundation for ISO 13485. In addition to software, our developers can work with you to create or tailor current features and modules to your company’s needs. Our integration service can enhance automation and process controls by connecting your equipment to our software with the Internet of Things (IoT). Each InstantGMP™ MD software license includes our Medical Device Standard Operating Procedures (SOPs).
Be sure to read this case study to learn about how InstantGMP™ MD can transform your operation: InstantGMP™ Customer Case Study (Docx format)
Additional Features & Benefits:
- Improve quality and consistency
- Track all records electronically
- Enhance traceability
- Reduce batch manufacturing complexity
- Avoid production interruptions
- Update inventory levels in real-time
- Scale batches at the click of a button
- And more!
Have questions? Want to talk to a live human being?
Hi, I’m Debbie Young, Medical Device Relationship Manager at InstantGMP, Inc. I’d love to tell you more about our fully-integrated software and how it can help you improve productivity.
You can email me (by completing the form on this page) or give me a call at (704) 302-3691.