One of the most common failures cited by FDA inspectors in Warning Letters is the…
Cary, NC – InstantGMP, Inc.’s InstantGMP™ MD electronic Device History Record software seeks to streamline Medical Device manufacturing.
InstantGMP™ MD is a viable alternative to available software suites on the market thanks to its unique quality-based workflow that lays the foundation for ISO 13485 compliance.
A Unique Software Solution
Designed from feedback from medical device manufacturers, InstantGMP MD™ is a cloud-based, fully validated software that is ready to use from day one. The newest version, v3.0, includes even more features and has the most up-to-date, user friendly interface available for manufacturers who must comply with 21 CFR part 820 and ISO 13485.
This software streamlines complicated medical device production with organized, electronic Device Master Records and Device History Records and built-in manufacturing controls derived from decades in quality assurance. While the software is a unique entry to the market, it features intuitive functionalities for module-by-module ease of use for beginners and experts alike.
”Since the beginning of InstantGMP in 2004, we have sought to make manufacturing FDA regulated products easy”, said, Dr. Richard Soltero, President of InstantGMP, Inc. “Now that we are introducing this latest version, we hope medical device manufacturers will find that going paperless has never been easier.”
To learn more about the software, check out the InstantGMP™ MD page.
InstantGMP, Inc. develops cloud-based electronic batch record software and SOPs that reinforce Good Manufacturing Practices. These software systems were developed to meet standards specific to the pharmaceutical industry and were recently updated for the Dietary Supplement, Pharmaceutical/Biotech, Medical Device, and E-Liquid industries. Please visit the Resource Center at InstantGMP.com for articles, and our Video section for tutorials on using our software or to view our GMP compliance series.