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The Patient Information Advisory Group (PIAG) was established in the United Kingdom under section 61〔(section 61 of the Health and Social Care Act 2001 )〕 of the Health and Social Care Act 2001〔(Health and Social Care Act 2001 )〕 and the Patient Information Advisory Group (Establishment) Regulations 2001〔(Statutory Instrument 2001 No. 2836: 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〔(Section 60 of the Health and Social Care Act 2001 )〕 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,〔(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. ==Terms of reference== The terms of reference for the PIAG were to: #Advise the Secretary of State on use of powers provided by section 60 of the Health and Social Care Act 2001, and in particular on: # *applications and proposals for use of these powers; # *draft regulations made under s60(1) of the Act; # *proposals to vary or revoke such regulations following the Secretary of State's required annual review of existing provisions. #Advise the Secretary of State on key issues, particularly those of national significance, relating to the processing of patient information. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Patient Information Advisory Group」の詳細全文を読む スポンサード リンク
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