CrO Biosciences, Inc., is an information management consulting firm located in Temecula, CA. We provide regulatory submissions, GCP inspection readiness, clinical trial support, and R&D Systems Exchange services to pharmaceutical, biotechnology, and medical device organizations.
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 trends so we ahead of the curve, every time. Our expert resources will help you to determine a successful forward-thinking strategy.
CrO Biosciences, Inc., is a global, woman-owned, operated and controlled company, which consists of regulatory and clinical operations professionals with over 60 years of combined experience.
Our goal is to become the most trusted organization by providing high quality, efficient, and effective services globally; while creating a personal touch with integrity and experience you can rely on.