Clinical Trial Protocol Development Services (CRO)

Every clinical investigation begins with the development of a clinical protocol. The protocol is a document that describes how a clinical trial will be conducted (the objective(s), design, methodology, statistical considerations and organization of a clinical trial,) and ensures the safety of the trial subjects and integrity of the data collected.

To meet these goals, the research protocol document includes the background, rationale, objectives, design, methodology, statistical considerations, and organization of the clinical research project.