· Feasibility evaluation by experienced clinical trial sites
· Non-disclosure and clinical trial agreements, suitability of trial sites selection and evaluation
· Trial finance, budgeting and costing
· Institutional Review Board and other regulatory
bodies document review and processing of trial protocols
· Recruitment and provision
of GCP trained trial coordinators and research nurses for trial sites or projects
· Collecting and arranging laboratory, cardiac and radiology investigations. Specific requests by sponsors for pharmacokinetic and pharmacodynamics
studies can be arranged or sourced for by sites
· Central laboratory and other requirements
for specimen/ radiology evaluation and testing can be arranged
· Documents for trials
can be archived and recalled when needed
· Site monitoring and audit, coordination
for trial sites to have regular reviews and updates
· Appropriate patient information
collection for trial purposes, follow up schedules for patients, case record reviews by clinician