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CHAPTER 37 IOWA PRESCRIPTION MONITORING PROGRAM 65737.1(124) Purpose and scope. These rules establish a prescription monitoring program (PMP) that compiles a central database of reportable prescriptions
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Rule 657-371 is designed to outline the requirements and processes for specific regulatory compliance in a designated field.
Entities or individuals who fall under the jurisdiction of the regulatory body associated with rule 657-371 must file this report.
To fill out rule 657-371, required forms should be accurately completed, ensuring all necessary information is provided, and then submitted as directed by the regulatory body.
The purpose of rule 657-371 is to ensure compliance with regulatory standards and to facilitate the monitoring of performance and practices in the relevant field.
The report must include specific operational data, compliance metrics, and any relevant performance indicators as mandated by the governing regulations.
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