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Regulatory Impact StatementHealth Records Regulations 2012Department of Health
May 2012
This Regulatory Impact Statement has been prepared in accordance with the
requirements of the Subordinate Legislation
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How to fill out this regulatory impact statement
How to fill out this regulatory impact statement
01
Start by providing the title and date of the regulatory impact statement.
02
Identify the purpose of the regulatory action and provide a concise summary of the proposed changes.
03
Clearly specify the objectives and expected outcomes of the proposed regulation.
04
Assess the costs and benefits of the regulatory action, including both monetary and non-monetary impacts.
05
Evaluate alternative options and explain why the proposed regulation is the most effective and efficient.
06
Consider potential risks and uncertainties associated with the regulatory action.
07
Provide a comprehensive analysis of the impacts on affected stakeholders, such as businesses, individuals, or government agencies.
08
Address any potential compliance or enforcement issues and propose a plan for monitoring and evaluation.
09
Include a consultation plan outlining how stakeholders were involved in the development of the regulatory impact statement.
10
Review and proofread the document before submission, ensuring it is clear, concise, and accurate.
Who needs this regulatory impact statement?
01
Regulatory impact statements are typically required by government agencies or departments responsible for developing and implementing regulations.
02
Policy makers, legislators, and decision makers use these statements to assess the potential impacts of proposed regulations and make informed decisions.
03
Stakeholders and interested parties also benefit from regulatory impact statements as they can understand the implications of new regulations on their operations or lives.
04
Anyone who wants to contribute to the regulatory process or provide feedback on the proposed regulation may also find these statements useful.
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