<?xml version='1.0' encoding='utf-8'?>
<regulation prefix="Regulation" num=".46" citation="COMAR 26.13.10.46" title_num="26" subtitle_num="13" chapter_num="10" heading="Standards for Healthcare Facilities Managing Potentially Creditable Hazardous Waste Pharmaceuticals.">
  <paragraph num="A.">
    <text>Hazardous Waste Determination for Potentially Creditable Pharmaceuticals.</text>
    <paragraph num="(1)">
      <text>A healthcare facility that generates a solid waste that is a potentially creditable pharmaceutical shall determine whether that pharmaceutical is a hazardous waste pharmaceutical by determining whether the waste is listed as a hazardous waste in COMAR 26.13.02.15—.19, and whether the waste exhibits any of the characteristics of hazardous waste defined in COMAR 26.13.02.10—.14.</text>
    </paragraph>
    <paragraph num="(2)">
      <text>In determining whether a solid waste is a hazardous waste, a healthcare facility shall follow the procedures in COMAR 26.13.03.02-1.</text>
    </paragraph>
    <paragraph num="(3)">
      <text>A healthcare facility shall use the hazardous waste determination conducted in accordance with this section to determine the applicability of Regulations .32—.49 of this chapter to the waste, except that the healthcare facility may choose to manage its potentially creditable non-hazardous waste pharmaceuticals as potentially creditable hazardous waste pharmaceuticals under Regulations .32—.49 of this chapter.</text>
    </paragraph>
  </paragraph>
  <paragraph num="B.">
    <text>Acceptance of Potentially Creditable Hazardous Waste Pharmaceuticals from Off Site.</text>
    <paragraph num="(1)">
      <text>This section establishes conditions under which a healthcare facility may accept potentially creditable hazardous waste pharmaceuticals from an off-site healthcare facility that qualifies, under federal regulations, as a very small quantity generator (VSQG) of hazardous waste.</text>
    </paragraph>
    <paragraph num="(2)">
      <text>Regulation .32F of this chapter specifies criteria that determine whether a generator of hazardous waste pharmaceuticals qualifies as a very small quantity generator of hazardous waste under federal regulations.</text>
    </paragraph>
    <paragraph num="(3)">
      <text>. For the purposes of this regulation:</text>
      <paragraph num="(a)">
        <text>“Person” has the meaning given by the definition in COMAR 26.13.01.03B; and</text>
      </paragraph>
      <paragraph num="(b)">
        <text>“Control”:</text>
        <paragraph num="(i)">
          <text>Means the power to direct the policies of the healthcare facility, whether by the ownership of stock, voting rights, or otherwise; and</text>
        </paragraph>
        <paragraph num="(ii)">
          <text>Does not include the situation when a contractor operates healthcare facilities on behalf of a different person.</text>
        </paragraph>
      </paragraph>
    </paragraph>
    <paragraph num="(4)">
      <text>A healthcare facility that does not have a permit or interim status that allows the facility to accept hazardous waste from off site may accept potentially creditable hazardous waste pharmaceuticals from an off-site healthcare facility if:</text>
      <paragraph num="(a)">
        <text>The off-site facility qualifies, under federal regulations, as a very small quantity generator (VSQG) of hazardous waste;</text>
      </paragraph>
      <paragraph num="(b)">
        <text>Either:</text>
        <paragraph num="(i)">
          <text>The receiving facility and the VSQG healthcare facility that is sending the potentially creditable hazardous waste pharmaceuticals off site are under the control of the same person, as specified in §B(3) of this regulation; or</text>
        </paragraph>
        <paragraph num="(ii)">
          <text>The receiving facility has a contractual or other documented business relationship whereby the receiving healthcare facility supplies pharmaceuticals to the VSQG healthcare facility; and</text>
        </paragraph>
      </paragraph>
      <paragraph num="(c)">
        <text>The receiving facility:</text>
        <paragraph num="(i)">
          <text>Is operating under the provisions of Regulations .32—.49 of this chapter for the management of the receiving facility’s potentially creditable hazardous waste pharmaceuticals;</text>
        </paragraph>
        <paragraph num="(ii)">
          <text>Manages the potentially creditable hazardous waste pharmaceuticals that it receives from off site in compliance with the requirements of Regulations .32—.49 of this chapter; and</text>
        </paragraph>
        <paragraph num="(iii)">
          <text>Keeps records of the potentially creditable hazardous waste pharmaceuticals that the facility receives from off site for 3 years from the date that the shipment is received, except that the periods of retention of these records is extended automatically during the course of any unresolved enforcement action regarding the regulated activity;</text>
        </paragraph>
      </paragraph>
    </paragraph>
  </paragraph>
  <paragraph num="C.">
    <text>Prohibition of Shipment.  Except for potentially creditable hazardous waste pharmaceuticals, a healthcare facility may not send hazardous waste to a reverse distributor.</text>
  </paragraph>
  <paragraph num="D.">
    <text>Biennial Reporting.  A healthcare facility is not subject to biennial reporting requirements under COMAR 26.13.03.06B with respect to potentially creditable hazardous waste pharmaceuticals managed under Regulations .32—.49 of this chapter.</text>
  </paragraph>
  <paragraph num="E.">
    <text>Record Keeping.  A healthcare facility that initiates a shipment of a potentially creditable hazardous waste pharmaceutical to a reverse distributor shall:</text>
    <paragraph num="(1)">
      <text>Keep the following records, in either a paper or electronic format, for each shipment of a potentially creditable hazardous waste pharmaceutical:</text>
      <paragraph num="(a)">
        <text>The confirmation of delivery; and</text>
      </paragraph>
      <paragraph num="(b)">
        <text>The shipping paper or papers prepared in accordance with 49 CFR Part 172 Subpart C, if applicable;</text>
      </paragraph>
    </paragraph>
    <paragraph num="(2)">
      <text>Unless the period of retention is extended in accordance with §E(3) of this regulation, retain the records identified in §E(1) of this regulation for at least 3 years from the date of shipment;</text>
    </paragraph>
    <paragraph num="(3)">
      <text>Maintain a record beyond the period specified in §E(2) of this regulation:</text>
      <paragraph num="(a)">
        <text>During the course of any unresolved enforcement action regarding the regulated activity; or</text>
      </paragraph>
      <paragraph num="(b)">
        <text>As requested by the Department or the Regional Administrator of Region 3 of the EPA; and</text>
      </paragraph>
    </paragraph>
    <paragraph num="(4)">
      <text>Ensure that any record required to be kept by this regulation is made readily available upon the request of an inspector representing the Department or the EPA.</text>
    </paragraph>
  </paragraph>
  <paragraph num="F.">
    <text>Response to Spills.  A healthcare facility shall:</text>
    <paragraph num="(1)">
      <text>Immediately contain a spill of a potentially creditable hazardous waste pharmaceutical; and</text>
    </paragraph>
    <paragraph num="(2)">
      <text>Manage clean-up materials from a spill of a potentially creditable hazardous waste pharmaceutical as non-creditable hazardous waste pharmaceuticals in accordance with Regulations .32—.48 of this chapter.</text>
    </paragraph>
  </paragraph>
</regulation>