WHEN YOU NEED A CLINICAL TRIAL EXPERT, ON CALL, AT YOUR SERVICE
Trial complexity is increasing at a rapid pace, and the services offered by traditional CROs are not keeping pace.
Biorasi’s consulting group is comprised of cross-disciplinary subject matter experts, including regulatory professionals, doctors, scientists, legal experts, and experienced clinical teams that work in tightly integrated groups to build better clinical development programs.
Biorasi’s consulting services are built around the idea that while individual trials and projects are important, ultimately they need to be part of an optimized and effective drug development program. We look at your projects in a global context, both figuratively and literally, and help you identify which pieces can be improved for success not just tomorrow, but a month or year or decade from now. Whether you need a quick answer to a CMC question or a specific regulatory requirement; a comprehensive clinical development plan or a study rescue assessment, Biorasi is ready to provide you with the resources you need.
Biorasi’s subject matter experts can keep you ahead of the curve, freeing your team to focus on creating new therapeutics and saving lives
Navigating Complex Trials to Approvals
Biorasi’s methodology leverages our TALOS Ecosystem, an integrated technology and program management platform designed exclusively for Clinical Research. The efficiency of the TALOS Ecosystem offers greater success for our sponsors and allows faster trial completion while minimizing risk of failure.
Biorasi has a solid track record of experience in dermatology, and our goal for this year is to share all corners of our knowledge on