Maryland Code § HG-21-2A-04

Section HG-21-2A-04
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(a) The Secretary, in consultation with the Board, shall adopt regulations
to carry out this subtitle.
(b) The regulations adopted by the Secretary shall:
(1) Specify the prescription monitoring data and naloxone
medication data required to be submitted under § 21-2A-03 of this subtitle;
(2) Specify the electronic or other means by which information is to
be submitted:
(i) Without unduly increasing the workload and expense on
dispensers; and
(ii) In a manner as compatible as possible with existing data
submission practices of dispensers;

(3) Specify that the information be submitted by dispensers once
every 24 hours;
(4) Specify that the Program:
(i) Shall provide the information technology software to
dispensers necessary to upload prescription drug monitoring data and naloxone
medication data to the Program; and
(ii) May not impose any fees or other assessments on
prescribers or dispensers to support the operation of the Program;
(5) Identify the mechanism by which:
(i) Prescription monitoring data are disclosed to a person, in
accordance with § 21-2A-06 of this subtitle; and
(ii) Naloxone medication data are disclosed to a person, in
accordance with § 21-2A-06.1 of this subtitle;
(6) Identify the circumstances under which a person may disclose
prescription monitoring data or naloxone medication data received under the
Program;
(7) Specify the process for the Program's review of prescription
monitoring data and naloxone medication data and reporting of:
(i) Possible misuse or abuse of a monitored prescription drug
under § 21-2A-06(c) of this subtitle; or
(ii) A possible violation of law or possible breach of professional
standards under § 21-2A-06(d) of this subtitle;
(8) Establish requirements for Program retention of prescription
monitoring data and naloxone medication data for 3 years; and
(9) Require that:
(i) Confidential or privileged patient information be kept
confidential; and
(ii) Records or information protected by a privilege between a
health care provider and a patient, or otherwise required by law to be held

confidential, be filed in a manner that, except as otherwise provided in §§ 21-2A-06
and 21-2A-06.1 of this subtitle, does not disclose the identity of the person protected.

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