Clinical trial monitoring is the process of overseeing the progress of a clinical trial, ensuring that it is conducted, recorded and reported in accordance with the study protocol, applicable Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the relevant regulatory requirements.
TechnoSTAT’s skilled clinical research associates (CRAs) ensure the highest quality of data review combined with effective communication with study sites both in Israel and abroad.
Our CRAs conduct on-site monitoring visits from initiation to close out visit (COV), performing the following services :
As your CRO, TechnoSTAT will manage the conduct of your trial to ensure proper clinical activities throughout the study.
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