Clinical Monitoring

SIRO offers high quality and deliverable based clinical monitoring services to manage a trial on time and on budget. Our experienced monitors manage and implement quality clinical trials using technology based solutions to provide a high level of expertise, efficient services and high end results to the pharmaceutical, bio-pharmaceutical and medical device industries.

• Projects on Oracle CTMS
• Experienced CTLs, Sr. CRAs and CRAs
• Strict adherence to SOPs

Our dedicated clinical monitoring team empowered with experienced CTLs /Sr CRAs / CRAs / documentation officers ensures ICH GCP compliance and data integrity during 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:

• Pre-study qualification visits
• Investigator site selection
• IRB submissions/approvals
• Organisation of training/start-ups meetings
• Clinical trial site management
• Clinical trial site monitoring and close outs
• Project logistic handling
• Query resolution
• Assessment visits (co-monitoring visits)

We have a robust in-house training and assessment program for each role within clinical monitoring to ensure the competency of our people as per project requirements. Monthly departmental meetings ensure the share of learning to each of the clinical monitoring team members across the projects which help in continuous up gradation of their technical and problem solving skills.