Celegence LLC is a global regulatory affairs consulting firm based in Downers Grove, IL. They specialize in providing operational and strategic consulting services to the life sciences industry, including pharmaceuticals, medical devices, and in vitro diagnostics. With their expertise in regulatory compliance, they help clients reduce costs and time to market by offering flexible and information-based solutions. Their innovative technology solutions, such as the CAPTIS MDR IVDR Compliance Tool and Dossplorer Viewer, streamline the process of creating regulatory documentation and managing regulatory dossiers. Celegence is dedicated to improving patient outcomes through intelligent regulatory compliance.
With a team of global regulatory consultants, Celegence offers up-to-date and robust regulatory intelligence to support product development and submission strategies. Their solutions and services provide clear visibility and control over diverse product portfolios, increased operational efficiency, lowered costs, and ongoing regulatory compliance. They also offer specialized services for EU MDR and IVDR compliance, helping device manufacturers navigate the complex regulatory landscape. Overall, Celegence is committed to helping their clients achieve unrealized efficiencies and maintain compliance in the ever-changing regulatory environment of the life sciences industry.
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