Quality Management System

Does My Pharmaceutical Organisation Need a QMS?

What Does GMPPro QMS Offer My Company?

How QMS Creates Consistency

Some of The Features of GMPPro QMS

• Change Control: Allows processes, procedures, materials, equipment, and documents to be changed and monitored at any time, improving the safety and quality of final products.
• Deviations/Incidents: Provides the tools to record vital information, such as batches, products, and descriptions of the events; circulation ensures that any relevant parties, are notified.
• Customer Complaints: Allows you to record customer requests and acknowledge areas of improvement, sparking quality investigations, and closing upon satisfactory conclusions.
• Product Returns: Guides a smooth workflow that starts with quality assurance inspection, inventory management, and reuse or preprocess tracking.
• Recall: Allows companies to access distribution lists, investigate, obtain approvals, and receive prompt recall notifications.
• CAPA Management: Corrective and Preventive Actions in GMPPro QMS help you improve your organisation’s processes and quality standards through effective identification, implementation, review and assessment of all actions which leads effective conclusion of incident or deviations.
• Supplier Qualification: Provides the right tools to ensure supplier quality and compliance based on certain performance metrics, allowing companies to create informed and reliable lists of approved suppliers and issue periodic evaluations for quality assurance.

Why Choose Motto’s QMS Services?

• Proven software development company with a proven Quality Management System (QMS).
• Ensures premium quality services and aligns with the ISO 9001 international standard.
• Customizes solutions based on client’s SOP, working around each company’s current operational framework.

Salient Features

• Designed to industry standards of high levels
• Easy deployment
• Automatic process notifications, escalations, routing and approvals
• Compatible to specific quality management processes
• Capable of launching CAPA, audit, complaints from any point in any process
• Accelerated responses to non-conformances and unexpected failures
• IQ and OQ Validation ready
• Tracking and monitoring processes and product performances throughout their lifecycle
• Real-time analytics
• Secure closed-loop management of validations, electronic signatures and reporting
• Configurable as licensed software on-premise or cloud-based
• Amenable to all regulatory requirements in force