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.

In general, for any pharma manufacturing process, it is important to have monitoring controls on entire production process, following departments are more essential.

GMPPro built with these five departments as a strong base and integrated from one department process to another department. In GMPPro, all multi department activities are well defined according to required regulatory norms like integrated Change management system, Deviation process, Investigations, Qualification & Approval processes.


    • Stores / Ware House
    • Production / Manufacturing
    • Quality Control
    • Quality Assurance
    • Engineering Services

    Planning & Procurement

    • Material Plan
    • Production Plan
    • Purchase Enquiry
    • Purchase Requisition
    • Purchase Order
    • Material Inward
    • Mixed / Tanker Solvents
    • Job Work Process
    • Inter unit Transfers
    • Material Pre-Inspection

    Material Inventory

    • Outward Process
    • Material Request & Release
    • Marketing Indents
    • Sales Quotations
    • Dispatch Advice
    • Product Dispatch
    • Supplier Management
    • Customer History
    • Bill of Materials
    • Batch Indents
    • Batch Line Clearance
    • Batch Process Records
    • BPR Request & Issue
    • Batch Execution
    • Electronic Batch Process
    • Recovery & Reprocess
    • Material Transfers
    • Commercial Packing
    • Dispatch Advice
    • Equipment Logs
    • Specifications
    • Sample Inward
    • Sample Analysis
    • Raw Data Management
    • Reserve Samples
    • In-house Working Standards
    • Reference Standards
    • Volumetric Solutions
    • Lab Chemicals
    • Out Of Specifications (OOS)
    • OOS Manufacturing Investigation
    • Out Of Trends (OOT)
    • Stability Protocols & Process
    • Certificate Of Analysis (COA)
    • Re-test Analysis
    • Instrument Calibration & Reports
    • Third Party Testing Samples
    • Samples Destruction
    • QA Release
    • Change Control
    • Deviations & Investigation
    • Incidents
    • Document Control
    • Supplier Qualification
    • Complaints
    • Product Returns
    • Audit Management
    • Training Management
    • Product Recall
    • CAPA Management
    • Quality Review
    • Yield Review
    • Electronic Document Management
    • Equipments
    • Instruments
    • Calibrations
    • Preventive Maintenance
    • General Maintenance
    • Service Request
    • Breakdown Maintenance
    • Equipment Occupancy
    • Work Permits
    • IQ, OQ & PQ Documents

    GMP Compliance for Life Science Industries

    Contact us for a demo & personal interaction