AMMPS Releases New Notification Form for Incidents and Potential Incidents Related to Medical Devices
Answers to your Questions
The newly issued form is intended for reporting:
Confirmed incidents linked to the use of a medical device
Potential incidents that could have led to harm under different circumstances
Malfunctions, performance issues, deterioration, or any defect that may compromise patient safety or device effectiveness
This initiative strengthens Morocco’s post-market surveillance framework and aligns with international best practices in medical device vigilance.
The AMMPS requires the form to be used by:
Medical device manufacturers and authorized representatives
Importers, distributors, and service providers
Healthcare institutions, clinics, and hospitals
Professionals involved in medical device maintenance, calibration, or operation
The form is now available on the AMMPS website and is required for all future reports concerning incidents or potential incidents related to MD.
You may also download the form directly from our website using the link above, or contact us via WhatsApp or email should you require it to be shared with you directly.
This standardized reporting process will:
Improve the consistency and quality of incident notifications
Facilitate faster analysis and corrective actions
Enhance patient safety and device performance monitoring
Strengthen compliance for all medical device operators in Morocco
We assist manufacturers, distributors, importers, and healthcare facilities in:
Preparing and submitting materiovigilance notifications
Setting up or improving post-market surveillance systems
Ensuring full compliance with Moroccan medical device regulations
If you need support in managing an incident notification or aligning your vigilance processes with AMMPS expectations, our team is ready to help.
