Quara Conseil supports you for your medical device regulatory needs. We offer comprehensive support for the creation of PMS (Post-Market Surveillance) and PSUR (Periodic Safety Update Report) documents, tailored to the specific class of your medical device and in accordance with European regulations. Our team of experts will work closely with you to ensure that all necessary requirements are met and that your PMS project is fully prepared. We look forward to the opportunity to assist your company in navigating the complex regulatory landscape of the medical device industry.