For the investigators who have large patient population and are interested in stepping in to the clinical research field as an investigative site, we will help prepare the site to conduct clinical trials.
Our Site Management Services includes:
- Finding the studies for the sites
- Feasibility
- Contract/Budget negotiation
- Regulatory documentation
- IRB approvals
- Preparing for site visits
- Site staff training
- Site and subject payments
- EDC/IVRS systems training
- Prepare source documentation
- Data entry
- Lab sample processing and handling
- Conduct quality assurance visits
- Site Audit and Inspection readiness