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.
Services
AREMA will help you to introduce many countries with right services and expertise.
Arema
in numbers
Years of Global Experience
0
+
Regulatory project
0
+
Happy global clients
0
+
Countries
0
+
Articles
December 12, 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
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 […]
December 11, 2025
Published by tlilir400@gmail.com on December 11, 2025
Categories
Pharmacovigilance en Afrique et au moyen orient La pharmacovigilance, une science ayant pour but de détecter, évaluer et prévenir les effets indésirables des médicaments, elle est […]



