Clinical institutions and investigators
Explore study feasibility, site readiness, clinical research coordination and prospective or retrospective projects. Discussions begin with institutional interests, the relevant cohort and the operational responsibilities appropriate to the proposed work.
Laboratories and pathology teams
Discuss project-specific pathology, testing, imaging and clinical-information support. The scope should make the performing party, applicable methods, documentation and review responsibilities clear.
Biospecimen and biobanking programmes
Explore authorised collection, sourcing, storage and specimen-management collaborations. The discussion covers permissions, material and information requirements, access, retention and transfer arrangements.
Start with the institutional fit
An initial conversation helps establish whether the research need, institutional permissions and delivery model are compatible. Any collaboration is agreed through the relevant institutional processes; an enquiry does not create an agreement or commitment.