Authorization from ANSM is required for drug / medical device products and manufacturers. We help you obtain and secure access to France in order to place products on the market legally. At Pharmassent we understand your challenges and know what is essential for you. Our specialists can save you valuable time by helping you with France ANSM (Agence Nationale de Sécurité du Médicament et des Produits de Santé) regulatory requirements. We can provide France and EU scale assistance with the development of your medical product. We can help you develop efficient collaborations with French authorities by providing customized high-quality solutions. To achieve this, we integrate our experience within our client’s operations and provide solutions specifically tailored to their requirements. As a result, our knowledge of scientific and legal issues with national competent authorities will help you move your product from the early stage of development through the entire French regulatory process and to a successful marketing authorisation.
