Clinical Monitoring

We offer high quality clinical monitoring services to manage trials on time and on budget.

Our dedicated clinical monitoring team ensure ICH GCP compliance and data integrity at each site visit, consistently retrieving high quality, on-time data. Our clinical monitoring team ensures adherence with standard operating procedures and strives to promote positive personal relationships with a high level of trust and confidence with all our customers.

Services offered include:

• Clinical trial site management
• Pre-study qualification visits
• Clinical trial site initiation
• Clinical trial site monitoring and close outs
• Project logistic handling
• Query resolution
• Assessment visits (co-monitoring visits)

CRAs with medicine, pharmacy, biology and other life sciences background trained in ICH GCP, local and international regulations are the main strength of the Clinical Operations department.

For more information, please contact us.