QMS

Quality Management System

Ensure compliance and efficiency with our QMS software, designed to document, track, and manage all your quality processes. From change controls to audit management, our system provides comprehensive oversight to maintain the highest quality standards.

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Why QMS tool ?

Quality is the foundation of every successful pharmaceutical product. Yet maintaining consistency across processes, documentation, and regulatory requirements can quickly become complex without the right tools. Amazig’s QMS module simplifies it all — bringing structure, traceability, and control to every step of your quality lifecycle. Our pharmaceutical quality management software centralizes critical data, automates quality processes, and ensures full compliance with evolving GxP and ISO standards. Whether you’re managing audits, CAPAs, or change controls, Amazig helps you maintain complete oversight and reliability — every day, across every team.

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  • Streamlined management of quality processes anddocumentation
  • Real-time visibility into compliance status andcorrective actions
  • Automated workflows that reduce manual errors andreview cycles
  • Centralized audit trails ensuring data integrityand transparency
  • Easy integration with RIM and IDMS modules forend-to-end control

Core features

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Customizable and flexible "à la carte" offer

Our system is composed of different modules developed to tackle speciic activities: they can either interact togetheror funtion independently. Pisck the one you want or go for the full package according to the needs, priorities and budget of your organisation.

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Centralized data with a user-centric approach

At Amazig, the user experience is at the center of our preoccupations. Each user journey has been carefully studied to be intuitive, requiring few to no training. We understand the complexity of the pharmaceutical environment and focus on offering the most agile and simple systems to our clients.

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Ready to optimize your ways of working and processes ?

FAQ

Does Amazig Systems provide regulatory consulting support?

Absolutely. Our experienced consultants support companies in managing regulatory dossiers, audits, and compliance processes.

Are Amazig Systems solutions compliant with international pharmaceutical regulations?

Yes. All our modules comply with standards such as FDA 21 CFR Part 11 and Good Manufacturing Practices (GMP).

Are training sessions included in the services provided?

Yes. Our training programs are tailored to the different roles within the pharmaceutical industry, helping users become quickly autonomous.

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Download the full Amazig brochure

Discover in details all the features and benefits of Amazig Suite. Download our comprehensive brochure to learn how our software can help you optimize to your processes.

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