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

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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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AREMA helps you enter new markets compliantly with the right expertise and services

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CTD
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Submission and registration

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Articles

August 28, 2026
Published by admin2 on August 28, 2026
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MOROCCO: NEW RULES FOR THE REGISTRATION OF USED OR REFURBISHED MEDICAL DEVICES

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.  […]
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