<?xml version='1.0' encoding='utf-8'?>
<regulation prefix="Regulation" num=".03" citation="COMAR 10.18.02.03" title_num="10" subtitle_num="18" chapter_num="02" heading="Definitions.">
  <paragraph num="A.">
    <text>In this chapter, the following terms have the meanings indicated.</text>
  </paragraph>
  <paragraph num="B.">
    <text>Terms Defined.</text>
    <paragraph num="(1)">
      <text>“Acquired immunodeficiency syndrome (AIDS)” has the meaning stated in Health-General Article, §§18-201.1(a) and 18-202.1(b), Annotated Code of Maryland.</text>
    </paragraph>
    <paragraph num="(2)">
      <text>“Anonymous” means that a patient does not use the patient's name as identification and can only be identified through use of a code.</text>
    </paragraph>
    <paragraph num="(3)">
      <text>“Assigned laboratory number” means a number assigned to a laboratory by the Department for use in filing reports of HIV infection or CD4+ count.</text>
    </paragraph>
    <paragraph num="(4)">
      <text>“Case” means an individual who has:</text>
      <paragraph num="(a)">
        <text>Been clinically diagnosed as having HIV or AIDS; or</text>
      </paragraph>
      <paragraph num="(b)">
        <text>Laboratory evidence of being infected by HIV.</text>
      </paragraph>
    </paragraph>
    <paragraph num="(5)">
      <text>“Clinical material” means:</text>
      <paragraph num="(a)">
        <text>An organism isolated from a clinical specimen;</text>
      </paragraph>
      <paragraph num="(b)">
        <text>Material derived or prepared from a clinical specimen in which evidence of a communicable disease has been identified or detected; or</text>
      </paragraph>
      <paragraph num="(c)">
        <text>If neither §B(5)(a) nor §B(5)(b) of this regulation is available, material from an individual already held by the medical laboratory, in the following order of preference:</text>
        <paragraph num="(i)">
          <text>A patient specimen;</text>
        </paragraph>
        <paragraph num="(ii)">
          <text>Nucleic acid; or</text>
        </paragraph>
        <paragraph num="(iii)">
          <text>Other laboratory material.</text>
        </paragraph>
      </paragraph>
    </paragraph>
    <paragraph num="(6)">
      <text>“Clinical or infection control practitioner” means a physician, infection control nurse, physician assistant, nurse practitioner, or other clinical staff designated by the administrative head of an institution to report under Health-General Article, §18-202.1, Annotated Code of Maryland.</text>
    </paragraph>
    <paragraph num="(7)">
      <text>“Department” means the Maryland Department of Health.</text>
    </paragraph>
    <paragraph num="(8)">
      <text>“Designated anonymous HIV test site” means an HIV counseling and testing site designated by the Department as a site where a patient may have an anonymous HIV test.</text>
    </paragraph>
    <paragraph num="(9)">
      <text>“Drug” means a drug that has been:</text>
      <paragraph num="(a)">
        <text>Licensed by the United States Food and Drug Administration (FDA); or</text>
      </paragraph>
      <paragraph num="(b)">
        <text>Approved by the FDA as an investigational new drug.</text>
      </paragraph>
    </paragraph>
    <paragraph num="(10)">
      <text>“Exemption” means a research project meeting certain criteria, with the result that no reporting is required under this chapter.</text>
    </paragraph>
    <paragraph num="(11)">
      <text>“Health officer” means the health officer in each of the 23 counties and the Commissioner of Health in Baltimore City or the duly designated representative of the health officer.</text>
    </paragraph>
    <paragraph num="(12)">
      <text>“Human immunodeficiency virus (HIV)” has the meaning stated in Health-General Article, §§18-201.1(a) and 18-202.1(b), Annotated Code of Maryland.</text>
    </paragraph>
    <paragraph num="(13)">
      <text>“Institution” means an entity that employs an individual licensed to practice osteopathy or medicine by the State.</text>
    </paragraph>
    <paragraph num="(14)">
      <text>“Institutional review board” means a group of individuals designated by an institution in compliance with 45 CFR Part 46 to review the use of human subjects in proposed research.</text>
    </paragraph>
    <paragraph num="(15)">
      <text>“Laboratory examination order” means the written document signed by a physician or other authorized individual that specifies one or more laboratory examinations to be performed in regard to a specified patient.</text>
    </paragraph>
    <paragraph num="(16)">
      <text>“Newborn HIV exposure” means a newborn infant whose mother has tested positive for HIV infection.</text>
    </paragraph>
    <paragraph num="(17)">
      <text>“Physician” means an individual licensed to practice osteopathy or medicine by the State or the physician's designee working under the supervision of the physician.</text>
    </paragraph>
    <paragraph num="(18)">
      <text>“Secretary” means the Secretary of Health or the Secretary's designee.</text>
    </paragraph>
  </paragraph>
</regulation>