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African Medical Devices Forum REPORTING FORM FOR COMPLAINTS FOR MEDICAL DEVICES INCLUDING IN VITRO DIAGNOSTICS For device end users all adverse events/product problems should be reported to the manufacturer
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Step 1: Visit the African Medical Devices Forum website.
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The African Medical Devices Forum is a platform that facilitates collaboration and information sharing among various stakeholders in the medical devices sector across Africa, focusing on improving safety, efficacy, and quality of medical devices.
Manufacturers, importers, distributors, and other stakeholders involved in the medical devices sector are required to file with the African Medical Devices Forum.
Filling out the African Medical Devices Forum typically involves submitting relevant information and documentation regarding medical devices, including details about the devices, manufacturers, and compliance with regulatory standards. Specific guidelines may be provided on the forum's website.
The purpose of the African Medical Devices Forum is to enhance regulatory harmonization, improve access to medical devices, ensure consumer safety, and promote best practices in the medical devices market across African countries.
Information that must be reported includes device specifications, safety data, manufacturing processes, importer and distributor details, adverse event reports, and compliance with regulatory requirements.
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