Cytespace delivers a range of services at sites in India for better site performance.
- Recruitment and development of Site Solutions Executives (SSEs) at clinical trial sites for specific studies
- Providing training on Good Clinical Practice (GCP), role and responsibilities, site Standard Operating Procedures (SOPs), therapeutic and protocol training, as mandated
- Deploy SOPs at every study-site (where required) and get sign-offs from the Prinicipal Investigator (PI)
- Support feasibilities and trial awareness programmes
- Patient pre-screening to help recruitment, eDC and query management, trial master file; study documentation upkeep, Investigational Product (IP) and supplies accountability
- Patient visit follow-up and compliance assistance
- Support monitoring visits and Quality Assurance (QA) audit action items
- Provide updates and site performance metrics to sponsors on an ongoing basis.
- Help optimize monitoring and reduce cost of poor quality data.