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<section article="gho" article_name="Health Occupations" number="12-6A-06" title_number="12" title_name="Pharmacists and Pharmacies" subtitle_number="6A" subtitle_name="Therapy Management Contracts">
  <level label="a">
    <text>A protocol under this subtitle:</text>
    <level label="1">
      <text>May authorize:</text>
      <level label="i">
        <text>For protocols by a licensed physician and licensed pharmacist, the initiation of drug therapy under written, disease–state specific protocols;</text>
      </level>
      <level label="ii">
        <text>The modification, continuation, and discontinuation of drug therapy under written, disease–state specific protocols;</text>
      </level>
      <level label="iii">
        <text>The ordering of laboratory tests; and</text>
      </level>
      <level label="iv">
        <text>Other patient care management measures related to monitoring or improving the outcomes of drug or device therapy; and</text>
      </level>
    </level>
    <level label="2">
      <text>May not authorize acts that exceed the scope of practice of the parties to the therapy management contract.</text>
    </level>
  </level>
  <level label="b">
    <text>A protocol shall prohibit the substitution of a chemically dissimilar drug product by the pharmacist for the product prescribed by the authorized prescriber, unless permitted in the therapy management contract.</text>
  </level>
  <level label="c">
    <text>A protocol that authorizes controlled dangerous substances drug therapy shall require the pharmacist to request relevant data from the Prescription Drug Monitoring Program before initiating or modifying a controlled dangerous substances drug therapy.</text>
  </level>
</section>
