We help companies that have identified a need for improvement in Clinical and Regulatory Operations. We have created processes for our clients in order to help them achieve agency approval for their applications.
Our first-hand experience has allowed us to deliver hands-on regulated content management assessment, guidance, and instruction for every major part of a life sciences company, from R&D document development, to Trial Master File (TMF) management and implementation, to Regulatory submissions.
Our unique methodologies are up-to-date with the latest rules, regulations, technologies and current industry and media trends so we ahead of the curve, every time.
CrO Biosciences is an information management consulting firm that provides clients with Inspection Readiness, regulatory submission planning and management. We have the expertise necessary to acquire agency approval for regulatory applications. We are a global, woman-owned, operated and controlled company, which consists of regulatory and clinical operations professionals with over 60 years of combined experience.