Do no harm: research should not expose subjects to direct harm
Benefits should outweigh the risk: Research should be worthwhile and provide value that outweighs any risk or harm
Researchers should aim to maximise the benefit and minimise harm to participants/patients and researchers.
Respect for autonomy
All participants in research must take part voluntarily, free from any coercion or undue influence
Their rights, dignity and autonomy should be respected and protected.
Equity: a core principle of justice in relation to research is equal treatment
Benefits should equally apply to everyone, and no one should be unduly burdened by the research.
Should not discriminate against any group
Informed consent: Informed consent requires participants to be given appropriate (a) information about the research (b) in a comprehensible manner (c) without duress or inappropriate inducement.
The information should include the procedure, purpose, risks and benefits, alternative procedures (where therapy is involved)
Need to offer the participant the opportunity to ask questions and to withdraw at any time from the research
Confidentiality & data protection: Individual research participant and group preferences regarding anonymity should be respected
Participant requirements concerning the confidential nature of information and personal data should be respected.
Integrity: research should be designed, reviewed and undertaken to ensure recognised standards of integrity are met and quality and transparency are assured
Usually involves the use of a review committee to ensure standards are being met
Conflict of interest: the independence of research should be clear and any conflicts of interest or partiality should be explicit
Using animals: There is a clear need to consider the care and treatment of animals as much as there is a need to consider humans