Clinical trial monitoring is the act 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 throughout the study to:
As your CRO, TechnoSTAT will manage the conduct of your trial to ensure proper clinical activities throughout the study.
Address: 34 Jerusalem Rd.
Beit Gamla -Bldg B, 5th Floor,
Raanana, 4350108 Israel