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Clinical Research Sites in Mexico

Clinical trials require strict adherence to protocol, extensive documentation, complete accuracy, compliance to ICH-GCP and other regulatory norms, an ethically patient recruitment strategy, and efficient site management.

PCR fulfills the need for a qualified team of clinical trial site management professionals who understand the intricacies of participating in global research projects. Our experience with the entire process from site evaluation, site initiation, site management and site closeout enables us to ensure timely and speedy responses at every stage of the study.

Site Management Organizarion (SMO)
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