Amazig platform

Amazig Systems offers a suite of intelligent software modules designed to help pharmaceutical companies navigate compliance, quality, and documentation requirements with confidence.

From regulatory management to document control, each module is built to support every stage of your product’s lifecycle — ensuring faster approvals, cleaner audits, and a streamlined path to market.

Choose the modules you need. Scale as your operations grow.
With Amazig, regulatory excellence becomes a daily routine.

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RIM (Regulatory Information Management) systemRIM (Regulatory Information Management) system

An integrated platform for managing regulatory content and data

Amazig Systems brings together all regulatory content, data, and processes within a single secure platform. Designed for pharmaceutical companies, it eliminates silos and ensures every stakeholder works from the same accurate, compliant information. From regulatory submissions to quality documentation, Amazig keeps everything synchronized and audit-ready.

By connecting your regulatory, quality, and documentation workflows, our software simplifies compliance and accelerates product approval — so your teams can focus on innovation, not administration.

Benefits

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With Amazig’s modular design, pharmaceutical companies can build a tailored regulatory environment that fits their exact operational needs. The platform enhances visibility across teams, reduces manual tasks, and supports faster, more reliable decision-making.

Each module — RIM, QMS, and IDMS — is designed to strengthen data integrity and traceability while reducing compliance risks. The result: shorter timelines, cleaner submissions, and total control over your regulatory information ecosystem.

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Why this is important ?

In the pharmaceutical industry, regulatory precision is not optional — it’s essential for product safety and market access. Yet, managing compliance manually exposes organizations to errors, delays, and costly inconsistencies.

Amazig provides the structure and automation needed to stay aligned with evolving global standards. By centralizing data and standardizing workflows, pharmaceutical companies gain both agility and confidence in every submission. Staying compliant becomes not just a requirement, but a competitive advantage.

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Regulatory compliance

Amazig systems are fully aligned with global standards such as Annex 11 of GMP and ISO 9001:2015

User-friendly interface

Our software presents an intuitive interface designed to fit the unique mindset of the users, with no extensive training required.

All-in-one solution

Amazig Suite offers a unified, cloud-based platform that enhances data visibility and accessibility.

Technical support

Our team is here to help you every step of the way, from implementation to daily business support.

Request a Demo

See Amazig Suite in action! Discover how our software can simplify your regulatory tasks, improve efficiency, and ensure compliance with a personalized demo. Let us show you how Amazig Suite can be tailored to your specific needs and request a custom quote. 

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