Research governance in health and social care: NHS permission for research and development involving NHS patients (second edition) (27th November 2008)
This document clarifies what primary care trusts need to consider before granting permission for research that involves NHS patients. For research under the Clinical Trials Regulations, the NHS decision to give permission should normally be a formality, provided sponsors confirm who is authorised to act on their behalf, supply evidence that the project has received the favourable opinion of a research ethics committee, authorisation by the MHRA and independent expert review, and give details of provisions to cover any liabilities.
Document
Permission Form for Industry Trials
This document clarifies what primary care trusts need to consider before granting permission for research that involves NHS patients. For research under the Clinical Trials Regulations, the NHS decision to give permission should normally be a formality, provided sponsors confirm who is authorised to act on their behalf, supply evidence that the project has received the favourable opinion of a research ethics committee, authorisation by the MHRA and independent expert review, and give details of provisions to cover any liabilities.
Document
Permission Form for Industry Trials
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