Mirette is a highly skilled regulatory affairs professional with 18 years of experience specializing in medical device regulatory affairs. Throughout her career, Mirette has been at the forefront of regulatory changes and has successfully navigated the evolving landscape of medical device regulations. Her extensive knowledge of regional regulatory requirements enables her to provide strategic guidance and support to organizations seeking to bring safe and effective medical devices to market. Mirette’s expertise spans a wide range of regulatory processes, including product classification, registration submissions, quality management systems, and post-market surveillance. She actively engages with regulatory authorities, industry associations, and other stakeholders to shape and promote best practices that prioritize patient safety and product quality as well to ensure compliance to the regulation in place. Her dedication to ongoing education and staying up to date with the latest regulatory developments allows her to effectively advocate for industry advancements while maintaining compliance. As a leader in her field, Mirette is known for her collaborative approach and ability to work seamlessly with cross-functional teams. She understands the importance of clear communication and building strong relationships with regulatory authorities, fostering an environment of trust and cooperation. With her 18 years of experience in medical device regulatory affairs, Mirette brings a wealth of knowledge and expertise to any organization. Her commitment to advocacy, shaping regulations, and ensuring compliance and product safety makes her a valuable partner in navigating the regulatory landscape and driving successful regulatory strategies.