
Medical Research and Research Governance
Research is vital in improving care and reducing uncertainty for patients now and in the future, and improving the health of the population as a whole. 1
A number of different activities come under the umbrella term of 'medical research'. This ranges from working in a laboratory with a microscope and cells, to investigations based on humans and patients in hospitals.
Medical Research can be grouped into 3 main categories:
- Clinical Audits
- Research (Clinical or Laboratory)
- Service Evaluation
- Clinical Audits: Aim is to see whether current standard of care is following pre-defined standards. Requires submission to RECs (Research Ethics Committee)
- Research: Aims to produce new knowledge to benefit patients in the future, and does not intend to directly benefit participants. Does not require REC approval.
- Service evaluation: Designed to define or measure current practise. Is not intended to be generalised beyond the setting at which the evaluation takes place. Does not require REC approval.
References
- General Medical Council (UK). Good Medical Practice: Probity and Research. October 2009.
http://www.gmc-uk.org/guidance/good_medical_practice/probity_research.asp - General Medical Council (UK). Good Medical Practice: Probity and Research. October 2009.
http://www.gmc-uk.org/guidance/good_medical_practice/probity_research.asp - General Medical Council (UK). Good Medical Practice: Maintaining Good Medical Practice. October 2009.
http://www.gmc-uk.org/guidance/good_medical_practice/maintaining_good_medical_practice_performance.asp - British Medical Association; Medical Ethics Today. London. BMJ Publishing Group, 2004.
- Declaration of Helsinki (2008 revision)
http://www.rdforum.nhs.uk/workgroups/primary/pcinfoguide/2ethics.htm - National Research Ethics Committee:
http://www.nres.npsa.nhs.uk/