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This document provides an initial statement of reasons for proposed amendments to the Disciplinary Guidelines within the California Code of Regulations, Title 16. It outlines the Board of Pharmacy's
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How to fill out 16 CCR § 1760 Initial Statement of Reasons

01
Identify the regulatory purpose for the initial statement of reasons.
02
Gather data and information relevant to the proposed regulation.
03
Outline the intended benefits of the proposed regulation.
04
Explain how the regulation aligns with existing laws and regulations.
05
Discuss any anticipated economic impacts on businesses or individuals.
06
Provide an analysis of alternatives considered during the decision-making process.
07
Include a summary of public comments received during the review period.
08
Draft the statement, ensuring clarity and compliance with legal standards.
09
Submit the completed initial statement of reasons to the appropriate agency.

Who needs 16 CCR § 1760 Initial Statement of Reasons?

01
State agencies proposing new regulations or amendments.
02
Regulatory bodies requiring justification for proposed changes.
03
Stakeholders involved in the regulatory process, including businesses and industry groups.
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16 CCR § 1760 refers to the Initial Statement of Reasons as a document prepared to outline the rationale behind proposed regulatory changes or new regulations within California Code of Regulations Title 16.
Typically, state agencies responsible for implementing regulations within their jurisdictions are required to file the Initial Statement of Reasons when they propose changes to the regulations.
To fill out the Initial Statement of Reasons, one must provide detailed information including the rationale for the regulation, the intended benefits, alternatives considered, and a summary of any data or evidence supporting the proposal.
The purpose of the Initial Statement of Reasons is to inform the public and stakeholders about the proposed regulatory action and to provide a basis for understanding the need for the changes.
The information reported must include the specific regulatory change being proposed, the legal authority for the proposal, the problem the regulation addresses, potential impacts, alternatives to the proposed regulation, and any relevant data or documentation.
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