The primary purpose of clinical monitoring is to protect the rights, safety, and well-being of study participants while ensuring the quality and integrity of the trial data. It involves on-site visits and remote monitoring activities to verify the accuracy and completeness of data collected during the trial.
​

• Site Initiation & Training

• Source Data Verification

• Adverse Event Reporting

• Protocol Compliance

• Data Integrity & Quality Control

• Commitment to Regulatory Compliance