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Laïla DIDOU has a diverse work experience in regulatory affairs and quality assurance roles. Laïla currently works at SociaNova as the Responsable des Affaires Réglementaires et Assurance Qualité - Software, where they are responsible for implementing the Quality Management System and ensuring CE marking conformity for their software.

Prior to this, Laïla worked at Caerus Medical and Endotact as a Spécialiste d'Affaires Réglementaires, where they defined regulatory paths, evaluated regulatory impacts of technological choices, and participated in the preparation of technical files for market approval.

Laïla also has experience as a Regulatory Affairs Officer - Implants du Rachis at Clariance Spine, where they managed regulatory documentation, facilitated FDA submissions, and handled international registrations in countries such as Japan, Mexico, USA, and Thailand.

Before transitioning into regulatory affairs, Laïla worked at DMS Imaging as a Regulatory Affairs Engineer, and at CIC-BT CHU Besançon in tissue engineering. Laïla also gained practical experience in radiology through a stage at Hôpital Cheikh Zaid Rabat.

Laïla's work experience demonstrates their expertise in regulatory affairs, quality assurance, and a diverse range of medical technologies.

Laïla DIDOU began their education in 2014 at the Université Internationale Abulcasiss Des Sciences De La Santé, where they pursued a field of study in Medical Imaging until 2017. Afterward, they attended ISIFC from 2017 to 2019, where they obtained a Master's degree in Biomedical engineering.