Presentation

AREMA specializes in regulatory affairs and pharmacovigilance, offering strategic and operational support to pharmaceutical, medical device, food and healthcare companies. Our expertise covers regulatory submissions, lifecycle management, and safety surveillance.

Geographical areas

With extensive experience across nearly 50 countries, AREMA is your trusted partner for navigating regulatory requirements and pharmacovigilance obligations worldwide. We support your product’s compliance and successful entry into several markets through tailored regulatory strategies, registration, and post-marketing safety services.

Arema
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Articles

December 12, 2025

Tunisia – New Version of the Human Medicines Registration Guide Published – June 2025

On June 4th, 2025, the National Agency for Medicines and Health Products (ANMPS) officially published the updated version of the Human Medicines Registration Guide in Tunisia. Download the […]
December 12, 2025

Tunisia: Publication of the Regulatory Compliance, Reliance, and Pharmacovigilance Guide

in June 2025, Tunisia’s National Agency for Medicines and Health Products (ANMPS) released a new official guide titled:  Regulatory Compliance, Reliance, and Pharmacovigilance Guide. The guide outlines the regulatory […]