Celeris Corporation conducts its business through three segments: Clinical Monitoring Services (CMS), Data Management Services (DMS), and Regulatory Consulting (RC). CMS clinical monitors on a contract basis to clients who assist clients in their clinical trials by ensuring that the records and data produced by a trial meet appropriate guidelines. DMS provides data management services on a contract basis to clients. These services ensure that the large amounts of data produced in clinical trials are properly collected and analyzed. In addition, the company has developed KnowledgePort™, a secure web portal that allows clients continuous access to study data. Through its subsidiary, C.L. McIntosh & Associates, Celeris provides regulatory consulting services, primarily to medical device and biologic manufacturers. The company assists manufacturers in obtaining and maintaining Food and Drug Administration clearance to market their products and to comply with all applicable FDA regulations. The company is based in Nashville, Tennessee.