W. Va. Code R. § 64-33-6 - Drug Procurement - Physician Eligibility
6.1. A physician is eligible to prescribe
delta-9- THC (marihuana) if he meets the following criteria.
6.1.1 The patient qualification review board
shall review and certify physician practioners for participation in the
controlled substances therapeutic research program.
6.1.2. Each physician desiring to participate
in the controlled substances therapeutic research program shall apply to the
patient qualification review board in a format prescribed by such board.
6.1.3. The physician shall
document experience in cancer therapy.
6.1.4. The physician shall have a current
drug enforcement administration controlled substances registration number.
6.1.5. The physician shall
register with a registered pharmacy as hereinafter described and the National
Cancer Institute.
6.1.6. The
physician shall affirm that the patient has signed an informed consent form. A
copy of such signed consent form shall be maintained by the patient
qualification review board.
6.1.7.
The physician shall limit drug usage to the purposes herein contained.
6.1.8. The physician shall report
adverse drug reactions immediately to the Investigational Drug Bank, National
Cancer Institute and to the patient qualification review board.
6.1.9. The patient qualification review hoard
shall issue a certificate of registry to each physician meeting the
requirements of these rules and regulations. The patient qualification review
board may revoke such certificate of registry for good cause shown. Those
affected persons desiring a public hearing shall do so in the manner prescribed
in and by the Rules of Procedure for Contested Case Hearings and Declaratory
Rulings, West Virginia Department of Health Procedural Rules, Series I, 1983.
The aforementioned rules of procedure are incorporated herein by reference.
6.1.10. Physicians wishing to
participate in the controlled substances therapeutic research program shall
register by completing and signing Federal Drug Administration Form 1573. Upon
certification by the patient qualification review board such Federal Drug
Administration Form 1573 shall be presented to a registered pharmacy which will
submit the form to the National Cancer Institute for approval.
6.1.11. The National Cancer Institute will
notify the applicant pharmacy of the physician's eligibility status and the
physician will be notified by the registered pharmacy.
6.1.12. Once certified, registered and
approved the prescribing physician shall complete a "Research Order for
Medication." The Research Order for Medication will be presented to a
registered pharmacy by the patient. Such Research Order for Medication is
identical to a prescription order. A standard prescription blank may be used,
but it must contain a statement that informed patient consent has been
obtained.
6.1.13. The quantity of
delta 9-THC dispensed is limited to 25 capsules (5mg strength) for each single
prescription.
6.1.14. The director
shall apply to contract with the National Institute on Drug Abuse or any
federally registered distributor or manufacturer for receipt of marihunana
pursuant to and in accordance with regulations promulgated by the National
Institute on Drug Abuse, the Food and Drug Administration and pursuant to the
provisions of these rules and regulations.
6.1.15. The director may cause such analyzed
marihuana to be transferred to a certified licensed pharmacy for distribution
to a certified patient upon the written prescription of a certified practioner
pursuant to the provisions of these rules and regulations.
6.1.16. The physician shall advise the
patient as to the effects and possible side effects of the drug (delta 9-THC)
prior to the initial administration thereof.
6.1.17. The director shall provide each
registered physician and registered pharmacy with a copy of the Group C
Guidelines for the use of Delta 9-Tetraydrocannabinol NSC 134454 for Nausea and
Vomiting Induced by Antineplastic Chemotherapy, September 1980, Investigational
Drug Branch Cancer Therapy Evaluation Program, Bethesda,. Maryland.
6.1.18. Delta 9-THC (marihuana) shall be
provided to each qualified patient pursuant to these rules and regulations at
no cost.
Notes
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