Assess the study before committing the work
A useful feasibility assessment connects the research question with the available cohort, records, sites and operational requirements.
- Study feasibility and cohort assessment, including available-record review.
- Hospital, investigator and research-site identification and assessment.
- Site readiness, operational planning, project timelines and budgeting.
Prepare for an organised start
We coordinate the working documentation and practical preparations needed for the agreed project scope.
- Startup and activation support, institutional agreements and working records.
- Training coordination, collection-kit readiness and site communication.
- Research-protocol and documentation support, including ethics-submission packs, participant information and consent materials.
- Coordination of amendments, institutional queries and continuing reviews.
Support continuity at site level
Research operations need attention between milestones as well as at them. We support authorised institutions with agreed participant and study coordination.
- Screening, recruitment, enrolment and participant follow-up coordination through authorised institutions.
- Prospective and retrospective projects, observational programmes and biospecimen-linked clinical studies.
- Matched-cohort and longitudinal operations, repeat timepoints and scheduled collections.
- Milestone reporting, issue escalation, operational quality review and reconciliation.
- Coded clinical information, study trackers, document review and missing-data queries.
Agree the responsibilities clearly
The engagement defines participating sites, institutional permissions, deliverables, communication routes and review points. Clinical care, medical decisions and institutional approvals remain with the appropriate authorised professionals and institutions.