Studies which require Sponsorship, a Legal Representative or other UK responsible person or organisation should follow the guidance on grant applications and sponsorship. The Joint Research Office will support UCL and UCLH researchers through the stages and approvals required to obtain any of these approvals. In some cases, a study will require a sponsor’s legal representative in the UK (Clinical Trials with a sponsor outside of the UK) or for some medical devices, a designated UK Responsible Person.Ī description of the responsibilities and requirements of each can be found on the HRA website. being jointly administered by the Office of Basic Research and the Office of. There are typically four stages of approval that must be considered and in place before conducting a clinical research project: All supported projects are university-based and unclassified, with the. UCL researchers with studies which fall outside of these categories should consult with UCL ethics.
To determine if your study requires any of the above approvals, refer to the HRA website. Research Databases and Research Tissue Banks Upon request of Managing authorities, JRC also provides policy and operational support for the structuring and management of science and technology parks, universities and Technology Transfer Offices (TTOs), incubators and accelerators to stimulate technology transfer for the benefit of regional economic development.The office reviews and approves studies classified as research and require any of the following: SICORP provides support for international joint research projects on the. The Joint Research Office supports researchers at UCL and UCLH. Office of International Collaboration, Division of International Strategy.
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