What is a CRO- A contract research organization (CRO) is a firm that manages clinical trials for the pharmaceutical, biotech, and medical device sectors.
Regulatory affairs, site selection, and activation, recruiting support, clinical monitoring, data administration, trial logistics, pharmacovigilance, biostatistics, medical writing, and project management are just a few of the services provided by CROs.
What is a CRO | Sponsors that Conduct a Set of Activities
CROs are engaged by sponsors to conduct a set of activities in a clinical study, taking on different technical and administrative obligations on their behalf.
What is a CRO | Organize | Coordinate | Execute Clinical Trial Procedures
The CRO's primary responsibility is to organize, coordinate, execute, and manage the procedures involved in the establishment of a clinical trial, serving as a point of contact for the sponsor and other trial participants (e.g. ethics committees, regulatory agencies, vendors, and hospitals).
CROs are important participants in clinical research since they have the expertise and capabilities required for a clinical study's proper development. Sponsors benefit from them since they save their burden while assuring trial quality and compliance with national and international standards.
At the same time, several CROs provide cutting-edge technology solutions to improve research process efficiency, resulting in cost savings.
CROs are undeniably important to the success of a clinical study. Sponsors should carefully examine their projects' unique requirements and seek out the CRO that best fits their technical demands and budget.
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