PRODUCT
DMS(Pro Dox)
A robust document ecosystem must have the dynamic capabilities to effectively manage the large volumes of data generated throughout operations. For companies in regulated industries, ensuring data security and accuracy is crucial to maintaining compliance with industry standards. GMPPro’s document control and management system is specifically designed to address these challenges, providing a secure and efficient platform for handling all documentation needs.
The system ensures that documents are easily accessible, securely stored, and accurately maintained throughout their lifecycle. It supports the secure retrieval, revision, and approval of documents as needed, while maintaining a complete audit trail for compliance purposes. With GMPPro, organizations can streamline document workflows, minimize the risk of errors, and ensure that all documentation meets the necessary regulatory requirements, helping businesses stay compliant and efficient in their operations.
GMPPro’s Document Management System (DMS) offers a reliable and efficient foundation for document control, simplifying and accelerating compliance processes. The solution enhances workflow efficiency and fosters collaboration across the organization, enabling teams to work together seamlessly towards achieving higher operational standards.
As an interconnected system, GMPPro’s DMS integrates with various quality systems and processes, ensuring smooth creation, storage, management, and distribution of documents within the organization. This unified approach streamlines document workflows, improves accessibility, and ensures that all documents are up-to-date, secure, and in compliance with industry regulations, ultimately driving improved performance and organizational success.


Features include, but not limited to
Document Hierarchy
Document Templates
Document Workflow
Document Life Cycle Process
Request & Issuance
Submission & Handover
Archival & Destruction
Document Reconciliation
Discover the Power of GMPPro Suite
Motto Systems’ GMPPro is a complete solution applicable to all pharmaceutical companies, small to large. Amenable for SOPs of the companies, integrating departments to clearly defined closed-loop QMS, incorporating all internal and external regulations effortlessly and seamlessly. Motto’s GMPPro conforms to 21 CFR Part 210 & 211 and EU annx. 11 guidelines.




Driving Efficiency and Compliance for Pharma Businesses Worldwide.
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