Publication date: 17 August 2026 Country: Morocco Domain: Medical Devices / Regulation  Morocco is strengthening its regulatory framework applicable to used or refurbished medical devices. A new ministerial order establishes the registration conditions for certain categories of these devices intended to be placed on the Moroccan market.  Devices concerned  The order establishes the registration conditions for certain categories of used or refurbished medical devices, including:  Medical imaging devices  External radiotherapy devices  Brachytherapy devices  Registration remains subject to compliance with the regulatory requirements set out in the order.  […]

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 […]

29 July 2026 | Source: Republic of Togo Togo is taking an important step toward strengthening its pharmaceutical regulatory framework. The Togolese authorities are currently finalizing […]

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, […]