June 18, 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 […]
June 4, 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 […]
June 3, 2025

Webinar: Training on eCTD in Tunisia – Basics of Electronic Submissions and Tunisian Regional eCTD M1

Arema is pleased to announce its participation in a training session presented with its partner EXTEDO  and in collaboration with the Tunisian National Chamber of the Pharmaceutical Industry (CNIP). […]
June 1, 2025

Reopening Of The Call For Applications For The Pilot Phase Of the Joint Evaluation Project Between the Egyptian Drug Authority (EDA) and the South African Health Products Regulatory Authority (SAHPRA)

The Egyptian Drug Authority (EDA) and the South African Health Products Regulatory Authority (SAHPRA) have announced the reopening of their joint pilot project for the collaborative […]
April 10, 2025

Tunisia: Pharmacovigilance, Urgent Deadline For Compliance With Regulation!

Tunisian National Agency for Medicines and Health Products (ANMPS) issued an urgent and important note by 10 April 2025 reminding all pharmaceutical companies to comply with pharmacovigilance […]
February 2, 2025

ALGERIA: Advancing Regulatory Digitalization in the Medical Device Sector

In an effort to enhance efficiency and transparency, the Algerian National Agency for Pharmaceutical Products (ANPP) has introduced key digitalization initiatives for the regulatory processes related […]