The act by a regulatory authority(ies) of conducting an official review of documents, facilities, records, and any other resources that are deemed by the authority(ies) to be related to the clinical trial and that may be located at the site of the trial, at the sponsor’s and/or contract research organization’s (CRO’s) facilities, or at other establishments deemed appropriate by the regulatory authority(ies).
About the Author: Manish Rauthan
This is Manish Rauthan and I am a Clinical Research Professional with Blogger and I am the owner of Clinical Ocean. Clinical Ocean is a blog for all the Clinical Research and Medical Professionals, specially for newbies who want to enter into CR domain. Follow me on twitter: @clinicalocean and Facebook ClinicalOcean