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This document outlines a legislative act aimed at enhancing the control and monitoring of prescription substances by requiring timely reporting and review of information regarding prescriptions of
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How to fill out Strengthen Controlled Sub. Reporting System

01
Access the Strengthen Controlled Sub. Reporting System application.
02
Create a user account or log in if you already have one.
03
Navigate to the reporting section of the application.
04
Collect necessary data regarding controlled substances for reporting.
05
Fill in the required fields accurately, including substance type, quantity, and usage.
06
Review the information for accuracy and completeness.
07
Submit the report for review by the relevant authorities.
08
Save a copy of the submitted report for your records.

Who needs Strengthen Controlled Sub. Reporting System?

01
Pharmacies and healthcare providers handling controlled substances.
02
Regulatory agencies monitoring controlled substance usage.
03
Hospitals and clinics that maintain records of controlled substance prescriptions.
04
Research institutions studying controlled substance impacts.
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All prescriptions for controlled substances shall be dated as of, and signed on, the day when issued and shall bear the full name and address of the patient, the drug name, strength, dosage form, quanti- ty prescribed, directions for use, and the name, address and registra- tion number of the practitioner.
(2) Controlled Substances (Schedules II, IIN, III, IIIN, IV, V) defined by the State and Federal Controlled Substances Acts may be procured, prescribed or ordered as established in the collaborative practice agreement, providing all of the following requirements are met: (A) the nurse practitioner has an assigned DEA
The NC Controlled Substances Reporting System (CSRS) collects information on dispensed controlled substance prescriptions and makes this information available to prescribers and dispensers.

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The Strengthen Controlled Sub. Reporting System is a regulatory framework designed to enhance the monitoring and reporting of controlled substances within a specific jurisdiction to ensure compliance and safety.
Entities involved in the manufacturing, distribution, or dispensing of controlled substances are generally required to file under the Strengthen Controlled Sub. Reporting System, including pharmacies, hospitals, and manufacturers.
To fill out the Strengthen Controlled Sub. Reporting System, organizations should follow designated procedures provided by the regulatory authority, which may include gathering relevant data, completing specific forms, and submitting them through an approved electronic or physical medium.
The purpose of the Strengthen Controlled Sub. Reporting System is to prevent misuse and diversion of controlled substances, improve accountability, and enhance public safety through comprehensive reporting and oversight.
The information that must be reported generally includes the type and quantity of controlled substances handled, records of transactions, and details regarding the patients or entities involved, along with any relevant compliance or incident reports.
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Relevant keywords

controlled substances North Carolina legislation prescription reporting healthcare drug monitoring Senate Bill Department of Health and Human Services real-time information prescriber requirements

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