Innovative, Paperless, Interactive, FDA Compliant Batch Management Software
InstantGMP™ PRO was designed for manufacturers of Pharmaceuticals, Biotech & Medical Devices. This software lays the foundation for compliance with 21 CFR Part 211 and 820, as well as ISO 13485,
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™ VAPE was created specifically for manufacturers of e-liquids for electronic cigarettes and complies with the compliance standards set by AEMSA & ISO 9001.
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.
Process 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™ software solutions 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.
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