Transforming Regulatory Compliance Through Innovative Solutions

Celegence provides regulatory affairs consulting and technology solutions to help life sciences companies navigate an increasingly complex regulatory landscape. With expertise across pharmaceutical, medical device, and in vitro diagnostic regulations, Celegence enables clients to bring safe, effective, and compliant products to market efficiently. Their services include regulatory labeling, publishing, IDMP and UDI compliance, medical writing, regulatory intelligence, and more. Celegence also offers proprietary software tools like CAPTIS and Dossplorer to streamline regulatory processes. Known for flexibility, domain expertise, and focus on compliance, Celegence serves as a trusted extension of clients' teams. They work with organizations of all sizes to reduce costs and time to market. Celegence's integrated approach allows for end-to-end management or modular support depending on needs.