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<section article="ghg" article_name="Health - General" number="21-2B-02" title_number="21" title_name="Food, Drugs, and Cosmetics" subtitle_number="2B" subtitle_name="Right to Try Act">
  <level label="a">
    <text>A manufacturer of an individualized investigational treatment operating within an eligible facility and in compliance with all laws applicable to an eligible facility may:</text>
    <level label="1">
      <text>Provide the manufacturer’s individualized investigational treatment to an eligible patient without compensation; or</text>
    </level>
    <level label="2">
      <text>Require an eligible patient to pay the costs of or associated with the manufacture of the individualized investigational treatment provided to the eligible patient.</text>
    </level>
  </level>
  <level label="b">
    <level label="1">
      <text>The Office of the Attorney General shall develop an informed consent form that:</text>
      <level label="i">
        <text>Complies with the requirements of § 21–2B–01(g)(3) of this subtitle;</text>
      </level>
      <level label="ii">
        <text>Includes instructions for the physician or patient on how to complete the form; and</text>
      </level>
      <level label="iii">
        <text>Provides spaces for a physician to include the information relating to a particular patient and the physician’s recommendation for the patient.</text>
      </level>
    </level>
    <level label="2">
      <text>This subsection may not be construed to prohibit a treating physician or a manufacturer of an individualized investigational treatment from including additional information or advisements with the informed consent form developed under paragraph (1) of this subsection.</text>
    </level>
  </level>
</section>
