Celegence specializes in providing flexible, information-based regulatory services and solutions. With regulatory expertise in medical devices, IVDs, and pharmaceuticals, our global consultants apply up-to-date intelligence and insight to support your product development and submission strategies. Celegence’s technology platform, CAPTIS, allows medical writers to simplify and expedite systematic literature reviews for EU MDR and IVDR compliance. This innovative solution reduces the industry resource burden by helping writers create and maintain compliant documentation with ease and consistency.