Patient Information Advisory Group

A non-departmental public body (arm’s-length body, quango) in the UK which was established under Section 61 of the Health and Social Care Act 2001, to advise on issues of national significance relating to the use of patient information and to oversee arrangements created under Section 60 of the Act, and subsequently under Section 251 of the NHS Act 2006, which permits the common-law duty of confidentiality to be set aside in specific circumstances for medical purposes.
PIAG provided the power and mechanism for ensuring that patient-identifiable information needed to support essential NHS activity—e.g., transferring personal health data to other organisations within the NHS—could be used without formal consent by the patients. PIAG drew its members from patient groups, healthcare professionals and regulatory bodies. PIAG was replaced by the National Information Governance Board for Health and Social Care (NIGB) under Section 158 of the Health and Social Care Act 2008. It was disbanded in 2008, and responsibility for administering Section 251 powers transferred to the NIGB in 2009.

a body established to advise the Secretary of State on any delegated legislation relating to the Secretary of State's powers to deal with patient medical information. Section 60 of the Health and Social Care Act 2001 provides a power to ensure that patient-identifiable information needed to support essential NHS activity can be used without the consent of patients. The power can only be used to support medical purposes that are in the interests of patients or the wider public, where consent is not a practicable alternative and where information made anonymously will be inadequate for the research.

单词	patient information advisory group
释义	Patient Information Advisory Group Patient Information Advisory Group A non-departmental public body (arm’s-length body, quango) in the UK which was established under Section 61 of the Health and Social Care Act 2001, to advise on issues of national significance relating to the use of patient information and to oversee arrangements created under Section 60 of the Act, and subsequently under Section 251 of the NHS Act 2006, which permits the common-law duty of confidentiality to be set aside in specific circumstances for medical purposes. PIAG provided the power and mechanism for ensuring that patient-identifiable information needed to support essential NHS activity—e.g., transferring personal health data to other organisations within the NHS—could be used without formal consent by the patients. PIAG drew its members from patient groups, healthcare professionals and regulatory bodies. PIAG was replaced by the National Information Governance Board for Health and Social Care (NIGB) under Section 158 of the Health and Social Care Act 2008. It was disbanded in 2008, and responsibility for administering Section 251 powers transferred to the NIGB in 2009. Patient Information Advisory Group Patient Information Advisory Group a body established to advise the Secretary of State on any delegated legislation relating to the Secretary of State's powers to deal with patient medical information. Section 60 of the Health and Social Care Act 2001 provides a power to ensure that patient-identifiable information needed to support essential NHS activity can be used without the consent of patients. The power can only be used to support medical purposes that are in the interests of patients or the wider public, where consent is not a practicable alternative and where information made anonymously will be inadequate for the research. AcronymsSeePIAG
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