Celegence LLC software

The Celegence team has extensive experience writing EU MDR & IVDR compliant documentation including Clinical Evaluation Plans & Reports and Post Market Surveillance Reports. Based on this experience, we have built a groundbreaking proprietary technology solution, CAPTIS™, to streamline MDR & IVDR document creation. With thorough knowledge of all aspects of Medical Writing, we offer an unparalleled end-to-end solution to ensure that you stay on track with post-market surveillance documentation. The CAPTIS™ solution can allow your team to streamline all aspects of your PMS documentation and avoid constant revisions. This not only improves efficiency and quality of medical writing teams, but also allows your RA project manager to quickly understand project status throughout the entire process.