Clinical Trial Monitoring
We offer deliverable based clinical monitoring services to manageclinical trials on time and within budget. Our experienced monitors manage clinical trial by implementing technology based solutions to provide efficient services and high end results to the pharma, bio-tech and medical device industries.
Our Dedicated clinical monitoring team empowered with experienced CTLs /Sr CRAs / CRAs / CTAs ensure ICH GCP compliance and data integrity. Our monitors performs both on site and off site monitoring visits. During each site visit our monitors identify and address issues in a timely fashion which ensures good quality and on-time data collection.
Our Clinical Trial Monitoring Services:
- Pre-study qualification/site selection visits
- IRB submissions/Regulatory submissions
- Investigator meetings/Start-ups meetings
- Clinical Trial Site Management
- Clinical Trial Site Monitoring and Close out visits
- Quality Assessment Visits (co-monitoring visits)