Monitoring
The purpose of the monitoring of a clinical trial is to verify that the rights of the subjects are protected, and to verify that the data reported are appropriate, complete, and verifiable source documents, and to verify that the conduct of the clinical trial is in compliance with the approved protocol, with the ICH/GCP and regulatory requirements in force.
Our Monitoring activities consist of:
- We develop Monitoring plans.
- We evaluated the centre pre-study and provide advice to Researchers.
- We do visits, initiation, monitoring interim and completion.
- We provide monitoring reports on time.
- We provide reports of information security.
- We handle documents of the trial.
Protection of subjects and compliance protocol.
We guarantee the protection of participants and the quality of the data, ensuring compliance with protocols and regulations.
- We guarantee that the rights of the subjects are protected throughout the clinical trial.
- We verify that the reported data are adequate, complete, and verifiable source documents.
- We ensure that the conduct of the clinical trial is in accordance with the approved protocol, the ICH/GCP and regulatory requirements in force.
- We guarantee compliance with the regulations and requirements applicable to the conduct of clinical trials, ensuring the validity of the results obtained.
We promote clinical research on a global level in Immunology
With these services, Immunoscience and positions itself as a reliable partner and are committed to the promotion of the continued growth of the Immunology and the advancement of the medical and scientific community to the global level.
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