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This document outlines the required equipment for testing sites administering skill tests for Medication Aide-Certified candidates and includes an affidavit certifying the availability of said equipment.
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How to fill out NEVADA MEDICATION AIDE–CERTIFIED TESTING SITE EQUIPMENT LIST AND AFFIDAVIT - FORM 1503CV

01
Obtain a copy of the NEVADA MEDICATION AIDE–CERTIFIED TESTING SITE EQUIPMENT LIST AND AFFIDAVIT - FORM 1503CV.
02
Review the list of required equipment for a certified testing site.
03
Ensure all equipment listed is present and in good working condition at your testing site.
04
Fill in the name of the testing site and the address on the form.
05
Verify that all equipment you have matches the specifications outlined in the form.
06
Sign and date the affidavit, affirming that the information provided is accurate.
07
Submit the completed form to the appropriate regulatory body.

Who needs NEVADA MEDICATION AIDE–CERTIFIED TESTING SITE EQUIPMENT LIST AND AFFIDAVIT - FORM 1503CV?

01
Individuals or organizations that operate a Medication Aide testing site in Nevada.
02
Training facilities that prepare candidates for the Medication Aide certification exam.
03
Regulatory bodies that require verification of equipment for compliance purposes.
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The NEVADA MEDICATION AIDE–CERTIFIED TESTING SITE EQUIPMENT LIST AND AFFIDAVIT - FORM 1503CV is a document used to certify and list the equipment available at testing sites for medication aides in Nevada.
Entities that operate certified testing sites for medication aides in Nevada are required to file this affidavit and equipment list to ensure compliance with state regulations.
To fill out the form, complete all required fields detailing the equipment available at the testing site, ensuring that all information is accurate and current before submission.
The purpose of the form is to ensure that certified testing sites meet the necessary equipment standards for training and evaluation of medication aides.
The form must report detailed information about the testing site's equipment, including types of items available, their condition, and any additional relevant details to verify compliance with regulatory standards.
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