Citation Tools
PDFResearch ethics
Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group
Download to a citation manager
Download the citation for this article by clicking on one of the following citation managers:
- Cite this article as:
- Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group
Other content recommended for you
- National survey of British public's views on use of identifiable medical data by the National Cancer Registry
- The social licence for research: why care.data ran into trouble
- Extracting information from hospital records: what patients think about consent
- Legal aspects of records based medical research
- Confidentiality and the duties of care
- Data protection, informed consent, and research
- Legal and ethical considerations in processing patient-identifiable data without patient consent: lessons learnt from developing a disease register
- Ethical approval for research involving geographically dispersed subjects: unsuitability of the UK MREC/LREC system and relevance to uncommon genetic disorders
- Non-commercial clinical trials of a medicinal product: can they survive the current process of research approvals in the UK?
- Preparing raw clinical data for publication: guidance for journal editors, authors, and peer reviewers