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Imperial as a sponsor
The College is responsible for
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- Research teams to access sufficient resources to deliver their research as proposed.
- The collection of high quality and accurate data.
- The management and monitoring of research, to ensure it is carried out in accordance with the approved protocol (or proposal) and regulatory requirements.
- Recording and reporting of significant developments as research proceeds, either in relation to the safety of individuals or scientific direction. In particular, ensuring appropriate arrangements for the recording and reporting of serious adverse events/reactions of any kind.
- Approving modifications to the design of clinical studies, obtaining any regulatory approvals and implementing them.
- The conclusion of a study, including plans for disseminating findings.
The College is also responsible for
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- Research proposals respect the dignity, rights, safety and well-being of participants and the relationship with care professionals.
- Only research of high scientific quality and good value for money is undertaken.
- An appropriate Research Ethics Committee has approved all clinical research projects.
- For clinical trials of investigational medicinal products, the Chief Investigator obtains a clinical trial authorisation and all trial arrangements comply with the law.
- All clinical research being undertaken through or within Imperial, including research undertaken by students as part of their training, is formally registered.
- The Chief Investigator and other key researchers have the necessary expertise and experience to conduct research as proposed.
- Agreement has been reached about compensation in the event of harm to research participants. For further information about this, please see our section on aircrack tutorial wep.
- Auditing or inspection by relevant authorities is permitted and assisted.