The Patient Information Advisory Group (PIAG) was established in the United Kingdom under section 61 of the Health and Social Care Act 2001 and the Patient Information Advisory Group (Establishment) Regulations 2001 to provide advice on issues of national significance involving the use of patient information and to oversee arrangements created under section 60 of the Act. Its membership was drawn from patient groups, health care professionals and regulatory bodies. Following the implementation of the Health and Social Care Act 2008, PIAG was abolished and its responsibilities transferred to a new body, the National Information Governance Board for Health and Social Care, with effect from January 2009.
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