Quality considerations at every stage.
Human biospecimen programmes require careful attention to ethical approvals, informed consent, protocol requirements, privacy, traceability, handling and transport. Clinfound coordinates with participating sites and project stakeholders to establish the documentation and processes required for each programme.
Company certifications include ISO 9001:2015, ISO 27001:2013 and ISO 20387:2018, as previously provided by the company. Certification scope, validity and issuing-body details should be verified before publication or reliance by a sponsor.
Collection and transfer are undertaken subject to applicable ethics committee approvals, consent permissions, institutional requirements, applicable law and contractual arrangements. Study-specific requirements are reviewed before work begins.
- Protocol-specific feasibility review
- Documented requirements and agreed responsibilities
- Coordination with participating investigators and sites
- Clear communication on project progress and constraints