PharmaCRO provides full package services for clinical trials, from developing protocols to clinical study reports,
and we also provide customized services based on what client needs.
PharmaCRO is committed to helping the successful completion of the most time-consuming processes of clinical trials and assisting in obtaining development product licensing in the most efficient way in the pharmaceutical, nutraceutical, and biotech industries.
We provide an overall range of services to clients, which include drug development consulting, developing protocols/case report forms, MFDS/IRB submissions and approvals, monitoring, clinical data management, statistical analysis and completing clinical study reports.
As our specialty is led by seasoned experts within the clinical research process, we are confident in our ability to comply with both local and international standards of regulations and Good Clinical Practice (GCP) standards.
PharmaCRO values the contribution it makes to improve standards of humanity through the successful development of Drug Candidates, Devices, Functional Foods and Cosmetics.