What We Do
How We Do It
How We Do It
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.
How We Do It
How We Do It
How We Do It
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 Strategy
How We Do It
Our Strategy
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.
Announcement
Welcome! CrO Biosciences is now an Emerging Services Partner of Veeva! Together, we’re collaborating to develop a series of service solutions to help you get ready and stay current with Veeva Vault solutions.