This is a healthcare certification masterclass that has been designed to help individuals build up a solid and a comprehensive framework in the medical device’s regulatory affairs, in partnership with Mecomed and Dubai Pharmacy College. The masterclass course is designed to equip participants with the real-world skills and knowledge required to be effective Regulatory Affairs professional in the medical device field.
It relies on a variety of training and facilitation methodologies and techniques used whenever applicable; these methods aim to enhance participant interaction while maximizing the learning journey.
Upon completion of this course, students/trainees will gain an extensive understanding about the important rules and regulations of the medical devices and the related authorities in the MENA Region, get an overview of the EU medical device regulations, gain understanding of the need of the medical device regulations and a comprehensive knowledge about the medical devices’ market in the MENA region. Apart from that, they will also learn the steps and procedures of the MD registration in each country separately and understand the technical dossier requirement and required certificates and how to obtain them (such as CE and ISO). Lastly, they will also get an overview of the importation procedures of the medical devices as per the competent authority and be able to understand the medical devices quality standards for the MENA region.