ZAMBIA: ZAMRA MAKES AVAILABLE 22 REGULATORY GUIDELINES COVERING HUMAN MEDICINES, PHARMACEUTICAL PRODUCTS AND CLINICAL TRIALS The Zambia Medicines Regulatory Authority (ZAMRA) has made available a collection […]

November 2026 training Activities at AREMA: eCTD Webinar & Regulatory/publishing Training In November 2026, AREMA International will participate in and organize two key activities focused on […]

Mastering the eCTD Format & New Regulatory Procedures in Tunisia: 2-Day Workshop AREMA is organizing a two-day training workshop dedicated to the eCTD format and the […]

Burkina Faso: The Faso Food and Drug Administration (Faso FDA) Officially Establishes Its Institutional Presence Regulatory Authority: Faso Food and Drug Administration (Faso FDA) Burkina Faso’s […]

Zimbabwe: MCAZ Announces Transition to eCTD Submissions by 2029 In its Circular No. 23 of 2026, dated 16 October 2026, the Medicines Control Authority of Zimbabwe […]

AREMA Takes Part in the 4th National Congress of Pharmacology in Tunisia Pharmacovigilance and regulatory developments: AREMA at the heart of professional discussions On 21, 22 […]

AREMA is pleased to announce its participation in the free webinar organized by EXTEDO, entitled “The eCTD Heatmap: Tracking Change Across GCC and Tunisia,” taking place […]

AREMA is pleased to announce its participation in CPHI Milan, taking place from October 6 to 8, 2026. We will be represented by our CEO, Zina […]

In March 2026, Burkina Faso’s Council of Ministers officially enacted the creation of the Faso Food and Drug Administration (Faso FDA), resulting from the merger of […]