Responsible for managing all EUDAMED modules, device registrations, post-market surveillance (PMS), and vigilance activities according to EU MDR 2017/745, Article 15. Ensures that device conformity checks are conducted in compliance with the implemented Quality Management System (QMS) before device release. Maintains and updates technical documentation and the EU declaration of conformity. Ensures compliance with post-market surveillance obligations.
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IBRAHIM Muhammad
Responsible for ensuring compliance with all regulatory requirements, including overseeing post-market surveillance and medical device vigilance. Lead clinical evaluations and manage risk to ensure the safety and effectiveness of medical devices. Oversee the registration of devices with competent authorities and ensure the implementation of a comprehensive Quality Management System (QMS) to maintain high standards of quality and regulatory compliance throughout the organization.
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Cartography of Glorious Mercantile Corp. (Pvt) Ltd