@ShahidNShah
Clinical monitoring and site management services delivered by our in-house CRAs
Our experienced CRAs support global and regional clinical trials through our comprehensive suite of clinical monitoring and site management services, from feasibility through to site closeout.
Feasibility Assessment
Study feasibility assessment
Country/Site recommendations
Site Identification and qualification
Site assessment
Review staff/investigator credentials
Collate documentation
Investigator Site Set Up & Initiation
Briefing/training of investigators, sub-investigators and staff
Initiation in study procedures and documentation
Site Management
Recruitment planning/tracking
IMP Management
Query resolution
Site Monitoring
Auditing
CQA Site audits are delivered by our CQA team
Site Closeout
Ensure completeness of study documentation
Closeout agreement and report
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