GMPPro is a software product from Motto Systems in compliance with international pharmaceutical standards.
GMPPro is a process accelerator.
Error free documentation with GMPPro.
We know the significance of seamlessly integrating the present and the future.
GMPPro helps you to future proof your business in long run.
End to end solutions for the pharmaceutical industry.
GMPPro the intelligence behind documenting science.
GMPPro is a new-generation software that focusses on error free documentation, customized to your own SOPs. Saves time, costs with optimized flow of your processes, backed by world class support.
Motto Systems has state of the art development facilities.
Motto Systems continuously explore the opportunities behind documentation in our quest to find affordable solutions and improve performance that benefits you as a pharma manufacturer.
Cost effective / Easier to use / More Reliable / Flexible / Fast / Service Focused
Your trusted partner in delivering complete document automation for Pharma For/Bulk Drug/Analytical/R&D
Face audits with ease. GMPPro software and reports are in compliance with 21 CFR Part 11 and can with stand the requirements of ICH / Who GMP / FDA / MHRA / TGA and other regulatory bodies.
Automated documentation with strict audit trails and security policies in place. These reduce the efforts needed to prove compliance to regulatory bodies enabling shorter approval life cycles.
Business of documentation simplified.

GMP Compliance for Life Science Industries

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