21 N.C. Admin. Code 46 .1607 - OUT-OF-STATE PHARMACIES
(a) In order to
protect the public health and safety and implement
G.S.
90-85.21A, the following provisions apply to
out-of-state pharmacies that ship, mail, or deliver in any manner a dispensed
legend drug, device, or medical equipment into this State.
(b) An out-of-state pharmacy may not ship,
mail, or deliver in any manner even a single dispensed legend drug, device, or
piece of medical equipment into this State until it receives a permit from the
Board. All unpermitted dispensing must be disclosed on any permit application,
and any permit applicant must update any application within 24 hours of any
dispensing into this State that occurs while a permit application is pending.
The Board may deny a permit based on that dispensing or on a failure to
disclose it.
(c) In addition to the
requirements contained in G.S. 85-21A, these pharmacies shall:
(1) supply all information requested by the
Board in carrying out the Board's responsibilities under the statutes and rules
pertaining to out-of-state pharmacies;
(2) during the pharmacy's regular hours of
operation but not less than six days per week, for a minimum of 40 hours per
week, provide a toll-free telephone service to facilitate communication between
patients and pharmacists at the pharmacy who have access to the patient's
records. This toll-free number must be disclosed on the label for each
dispensed drug, device, or piece of medical equipment;
(3) comply with all USP and FDA requirements
regarding the storage, packaging, and shipping of drugs, devices, and medical
equipment;
(4) develop policies
governing:
(A) normal delivery protocols and
times;
(B) the procedure to be
followed if the patient's drug, device, or medical equipment is not available
at the out-of-state pharmacy, or if delivery will be delayed beyond the normal
delivery time;
(C) the procedure to
be followed upon receipt of a prescription for a condition that requires
treatment before the drug, device, or medical equipment would be delivered in
the normal delivery time, which shall include a procedure for delivery of the
drug, device, or medical equipment to the patient from the out-of-state
pharmacy at the earliest possible time (such as courier delivery), or an
alternative that assures the patient the opportunity to obtain the drug,
device, or medical equipment at the earliest possible time; and
(D) the procedure to be followed when the
out-of-state pharmacy is advised that the patient's drug, device, or medical
equipment has not been received within the normal delivery time and that the
patient is out of the drug, device, or medical equipment and requires interim
dosage until the pharmacy can provide the drug, device, or medical
equipment;
(5) disclose
the location, names, and titles, of all officers and direct and indirect owners
of the pharmacy. Disclose the names and license numbers of all pharmacists
dispensing drugs, devices, or medical equipment to an ultimate user in this
State, the names and, if available, license or registration numbers of all
pharmacy personnel employed by the out-of-state pharmacy who assist pharmacists
in dispensing. The pharmacist-manager for the out-of-state permit issued by
this Board must be the same person as the pharmacist-manager (whether called a
pharmacist-manager, a person-in-charge or otherwise) of the pharmacy on the
permit issued by the pharmacy's home state. A report containing this
information shall be made on an annual basis and within 30 days of each change
of any pharmacist-manager, officer, or owner (whether direct or indirect) of
the pharmacy. A new permit shall be required under the circumstances set out in
Rule .1603 of this Section, and a new permit must be secured before any legend
drugs, devices, or medical equipment may be dispensed into the State of North
Carolina following any of the enumerated changes in circumstances. The existing
permit becomes void upon one of the events in Rule .1603, and any dispensing
into the State of North Carolina following one of those events is unlawful and
grounds for denial of a new permit;
(6) submit evidence of possession of a valid
license, permit, or registration as a pharmacy in compliance with the laws of
the state in which the pharmacy is located;
(7) designate a registered office and
registered agent in North Carolina for service of process pursuant to Article 4
of Chapter 55D of the North Carolina General Statutes. The Board may serve or
deliver any notice or other document provided for under the Pharmacy Practice
Act or these Rules on that registered agent. The Board may further serve or
deliver any notice or other document provided for under the Pharmacy Practice
Act or these Rules on the Secretary of State when the Secretary of State
becomes an agent of the entity pursuant to Article 4 of Chapter 55D of the
North Carolina General Statutes; and
(8) notify the Board within five days of
receipt of any order or decision by a Board of Pharmacy or other state or
federal agency imposing discipline of any sort on the pharmacy, or receipt of
any warning letter from the Food and Drug Administration.
(d) The facilities and records of an
out-of-state pharmacy shall be subject to inspection by the Board. The Board
also may require submission of inspection reports by the licensing entity of
the state in which the pharmacy is located or records transmitted by the
pharmacy to the Board offices.
(e)
Any person who ships, mails, or delivers prescription drugs to North Carolina
residents from more than one out-of-state pharmacy location shall register each
pharmacy separately.
(f) An
out-of-state permit holder may be disciplined as set forth in the Pharmacy
Practice Act. The suspension or revocation of the pharmacy's home state permit
will result in the immediate suspension or revocation of the out-of-state
permit issued by this Board.
(g) An
out-of-state pharmacy permit shall expire on December 31 of each
year.
(h) The fees provided for in
G.S.
90-85.21A as maximum fees which the Board is
entitled to charge and collect are hereby established as the fees for each
original permit and for annual renewal of each permit.
Notes
Eff. July 1, 1994;
Amended Eff. March 1, 2006;
Pursuant to G.S. 150B-21.3A, rule is necessary without substantive public interest Eff. October 3, 2017.
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