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
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[…]
In the newest version of InstantGMP, we’ve added a multitude of new features and updated existing ones to make them more efficient for users. New Client Features The Client menu is now under the Administration module and no longer on the Projects sub-menu. This allows for a user to input their client information much earlier[…]
Cary, NC – InstantGMP announces the release of v2.052 with amazing new features InstantGMP, Inc. added many great new functions and updates to their electronic batch records software to enhance their user’s experience. “We are excited about the new master production record and batch production record features in our v2.052 release” said Dr. Richard Soltero,[…]
New Functionalities Expanded badge signature capabilities to system-wide usage. Added new workflows focused on Project Management functionalities allowing for projects to include multiple products for multiple clients with multiple user access control under multiple roles. Added new Material Classifications to help employ naming conventions for incoming materials versus outgoing manufactured, packaged or labelled WIPs or[…]
The acting deputy director of the Division of Dietary Supplement Programs at the FDA, Cara Welch, Ph.D., left the author of this article with some confusing takeaways: If you are a Dietary Supplements manufacturer who wants to learn good manufacturing practices, read the GMPs for dietary supplements and apply them, otherwise, you are at risk[…]
E-cigarettes will soon be regulated under tobacco products as a rule proposed by the Food & Drug Administration (FDA). The rule is currently being reviewed by the White House Office of Management and Budget’s Office of Information and Regulatory Affairs. It will be several weeks before the proposed rule is formally approved and any action[…]
From Natural Products Insider, health food sales in China are estimated to reach RMB300 billion ($47.5 billion USD) by 2019. More and more Chinese consumers are looking to health supplements as rates for certain illnesses such as lung cancer and breast cancer are on the rise, and they are looking to purchase foreign health products.[…]