Project Development and Implementation
Excellence by design
The success of a clinical trial begins with qualified, experienced monitors to implement your project. Our research professionals have expertise in multiple therapeutic areas and with Phase 1 to Phase 4 clinical trials, and can assist you in setting up and initiating your clinical programs.
To ensure a smooth-running trial, each project is carefully planned, the management team individually selected, and specialized training conducted for the team, investigators and monitors.
Services
- Protocol design and development
- Preparation of informed consents
- Development, design, and printing of case report forms
- Identification of investigators
- Site qualifications
- Collection and processing of regulatory documents
- Writing of monitoring plans
- Writing of CRF completion guidelines
- Design of study specific screening & enrollment logs
- Design of study specific drug accountability and dispensing logs
- Management of EDC (electronic data capture) trials