Cary, NC – InstantGMP, Inc.’s InstantGMP™ PRO electronic batch record software seeks to streamline Pharmaceutical & Biotech manufacturing.
With its new sleek design and user friendly interface, version 3.0 of InstantGMP™ PRO aims to change the pharma manufacturing landscape with guided, intuitive modules.
InstantGMP PRO™ v3.0 is the brainchild of Dr. Richard Soltero based off of over 40 years of pharmaceutical manufacturing experience. The software comes fully validated, and complies with the 21 CFR Part 11 and 211 requirements for pharmaceutical & biotech production.
The software was designed to alleviate the burden of record keeping by manufacturers, improve quality and consistency, and automate the manufacturing process in an effort to maximize efficiency.
”We are very excited about this new release of our software” said Dr. Soltero, President of InstantGMP, Inc. “The software has been evolving for the past 12 years and this latest iteration is designed to significantly enhance our user’s experience and to make their production life easier”.
To learn more about the software, check out the InstantGMP™ PRO 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.