Presentation

AREMA specializes in Regulatory Affairs and pharmacovigilance, offering strategic and operational support to pharmaceutical, medical device, food and healthcare companies. Our expertise spans regulatory intelligence, regulatory submissions, lifecycle management, and safety surveillance; covering every stage of your product’s journey from development to post-market

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.

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Articles

June 2, 2026

Pharmacovigilance In Tunisia

The Tunisian ANMPS has published a new questionnaire addressed to Marketing Authorization Holders (MAHs) as part of the ongoing strengthening of Pharmacovigilance and regulatory compliance activities in Tunisia. This initiative further highlights the importance of maintaining robust local PV oversight and effective regulatory support through qualified local partners.   These two questionnaires were developed to collect accurate and relevant information to guide future actions, improve current practices, […]

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