Our Software Solutions
InstantGMP™ offers a variety of software solutions for manufacturers who make products regulated by GMPs
InstantGMP™ VAPE was created specifically for manufacturers of e-liquids for electronic cigarettes and complies with the compliance standards set by AEMSA & ISO 9001.
InstantGMP™ MES was designed for manufacturers of dietary supplements. This software was designed to reinforce good manufacturing practices (cGMPs) for 21 CFR 111 & ISO 9001.
InstantGMP™ MD was designed for manufacturers of medical devices and comes fully validated. This software lays the foundation for compliance with ISO 13485 & 21 CFR Part 820.
InstantGMP™ PRO was designed for manufacturers of pharmaceuticals & Biotechnology. It comes fully validated. This software lays the foundation for compliance with 21 CFR Part 211.
GMP & QA Consulting Services
Our focus is making cGMP compliance easy and our goal to help you find reasonable, cost effective ways of meeting, implementing or improving your cGMP compliance to meet FDA requirements.
Customization & Integration
InstantGMP™ MD & PRO can be customized to fit your specific needs. Our software experts will help you define your requirements and provide a customized solution that is built on the foundation of the existing software systems.
Standard Operating Procedures
InstantGMP™ has numerous Standard Operating Procedures & Policies available for purchase. Both the software and SOPs/Policies from InstantGMP provide the foundation for a total quality system.
Who we are
InstantGMP™ develops cloud based electronic batch record software and SOPs that reinforce Good Manufacturing Practices. We are manufacturing and quality experts dedicated to developing a unique solution for organizing batch records and managing GMP work flows that automatically maintain compliance while manufacturing FDA regulated products. Our software and GMP expertise is available to help you with custom applications and integration with other software. Our mission is to make GMP manufacturing easy.
Years in Software Development
% of customers that pass their FDA audits
Benefits of InstantGMP
InstantGMP™ was engineered to simplify manufacturing compliance
The Food and Drug Administration seeks to speed up the review of medical devices with a new premarket pilot program. How does the FDA handle premarket approval now? The FDA uses a group of reviewers from the Office of Device Evaluation (ODE), and the main issue with that is that the pool is populated by[…]
The San Jose Mercury News reports that California is the 2nd state to raise the legal smoking age from 18 to 21 as of a Thursday state Assembly vote. The lawmakers also tightened and closed existing loopholes in smoke-free workplace laws and now require all K-12 schools be tobacco-free. The bill was written and cleared[…]
Hank Schultz wrote up a piece via Nutra Ingredients USA that the FDA sent out warning letters to eight companies marketing dietary supplements containing CBD. The letters also mention illegal drug claims based on CBD being the active ingredient in two drugs currently in development. What is CBD? Cannabidiol (CBD) is a fraction of the[…]
House Bill 1432 authored by an Indiana Representative Kevin Mahan is turning heads. The Bill is looking to set a legal definition of an e-liquid, and require manufacturers of e-liquids to undergo rigorous standardization lest incurring civil or criminal penalties. Portions of the bill have passed and are slated to go into effect in July[…]
Dear InstantGMP Users, We have updated InstantGMP™! Version 2.054.001 has been released and your instances have been updated. Improvements Automatic conversion of Unit on BPR Instructions to Material Unit. Automatic conversion of Unit on BPR Instructions Usage on multiple lines to Material Unit. Fixes On some instances when Inventory levels where above 100% the application[…]
New Functionalities New MPR and BPR workflow allows users to navigate between manufacturing instruction steps without scrolling on summary page. New BPR functionality automatically checks for quantity used of material on each step for defined range. Added option to Unlock “Locked” MPRs and make edits. Signature and comment log retained for that version. Introduced Medical[…]
Cynthia Cabrera from the Contra Costa Times offers a great guest commentary on vaping: it’s not the same as tobacco and shouldn’t be treated as such. According to new information from the Centers for Disease Control and Prevention confirm that vapor and e-cigarette products are causing a reduction in the amount of smokers. Research also[…]
Thanks for joining InstantGMP for our new feature series. We are excited to launch IGMP 2.052 with streamlined workflows, more options and more smart fields! We have incorporated industry expertise, customer feedback and new capabilities in order to make your job as a Quality Manager, Project manager, Production supervisor or operator easier. There is a[…]
How is the new version of our Manufacturing Execution System different? Check out this handy infographic for a list of new functionalities, features, and fixes!
We’ve made a number of changes to the Master Production Record. Here you will find a great primer for everything coming in the latest update. The status of an MPR is now in the leftmost column and MPRs can now be approved or rejected. There are four statuses: Approved, Locked, in-Progress, and Rejected. Approved: All[…]