Cary, NC – InstantGMP, Inc.’s InstantGMP™ Vape v3.0 is sporting a new look. This quality-based software for e-liquid manufacturers now features a more intuitive and user-friendly experience while improving upon its scaling and formulation adjustment functionalities.
”We are very pleased to introduce version 3.0 of InstantGMP™ Vape to the e-liquid manufacturing community”, said Dr. Richard Soltero, President of InstantGMP, Inc. “We are proud to support these manufacturers who have made a commitment to quality by following the FDA’s Good Manufacturing Practices.”
Amazing New Look
InstantGMP™ Vape Version 3.0 features a completely redesigned user interface with multiple blue hues and with straight-forward buttons and icons for improved user experience. Additionally, users can create their own preferences while using the software for even more accessibility.
Most notably, users can easily scale their batches up or down with mere clicks of a mouse and the new yield will auto-populate the recipe quantities and the amounts to be measured out during production. Formulation adjustment has been simplified, thus allowing manufacturers to make changes and reap time-saving benefits.
This software is in compliance with the forthcoming FDA regulations for E-Liquid manufacturers. To learn more about the new look, functionalities, and features; check out the InstantGMP Vape 3.0 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.