Fla. Admin. Code Ann. R. 64B16-28.850 - Special Pharmacy - ESRD
(1) An
ESRD Pharmacy is a type of special pharmacy as provided by Section
465.0196, F.S., which is limited
in scope of pharmacy practice to the provision of dialysis products and
supplies to persons with chronic kidney failure for self-administration at the
person's home or specified address. Pharmacy services and dialysis supplies and
products provided by an ESRD pharmacy shall be limited to the distribution and
delivery of legend drugs included in schedule subsection (3), below; or legend
devices included in schedule subsection (4), below; which are ordered by a
physician for administration or delivery to a person with chronic kidney
failure for self-administration at the person's home or specified address. All
dialysis supplies and products provided by an ESRD pharmacy shall be
prepackaged and shall be covered by an approved NDA or 510 (k) application
issued by the Federal Food and Drug Administration.
(2) Prior to engaging in an ESRD pharmacy
practice an entity shall obtain a special ESRD pharmacy permit as provided
herein.
(3) Schedule of legend
drugs:
(a) Saline Solutions.
(b) Porcine Heparin.
(c) Beef Heparin.
(d) Dextrose Solutions.
(e) Doxercalciferol.
(f) Epoetin Alfa.
(g) NACL INJ 50 MEQ/20 ML.
(h) Levocarnitine.
(i) Lidocaine.
(j) Vitamin Preparations (dialysate use
only).
(k) Paricalcitrol.
(l) Peritoneal Dialysate Solutions.
(m) Protamine Sulfate.
(n) Potassium 20 MEQ/10ML (dialysate use
only).
(o) Sodium Ferric Gluconate
Complex or equivalent.
(p) Sterile
Water for Irrigation.
(4)
The schedule of legend devices includes:
(a)
Hemodialyzers.
(b) Hemodialysis
solutions.
(c) Bloodlines and
Associated Connectology.
(d)
Peritoneal Dialysis Tubing and Connectology.
(5) The provision of legend drugs and devices
included in the schedule necessary to perform dialysis to a person with chronic
kidney failure for self-administration at the person's home or specified
address shall be under the professional supervision of an appropriate
practitioner licensed under Florida law. The consultant pharmacist shall assure
that the following occurs:
(a) The ESRD
pharmacy receives a prescription from the prescribing practitioner directing
the pharmacist to dispense and deliver to a person with chronic kidney failure
(or such person's designee) any legend drugs and/or devices included in the
formulary necessary for the self-administration of dialysis at such person's
home or specified address.
(b) That
no dispensing shall occur unless the person with chronic kidney failure has
been trained in the proper use and administration of such products. Further,
the consulting pharmacist shall ensure that the ESRD pharmacy has received
records confirming the completion of such training.
(c) After the delivery of such products by
the ESRD pharmacy, the ESRD pharmacy shall upon request therefor, make
available to the prescribing practitioner documentation describing, in
sufficient detail, the types and quantities of products dispensed and delivered
by the ESRD pharmacy. The ESRD pharmacy shall also, upon request, make
available to the prescribing practitioner documentation confirming shipment of
such products and receipt thereof by the person with chronic kidney
failure.
(6) The licensed
ESRD pharmacy shall comply with all applicable state and federal regulatory
requirements and shall maintain in effect all applicable permits and licenses
required to dispense and deliver legend drugs and/or devices included in the
formulary described in this Section.
(7) The ESRD pharmacy shall deliver products
to a person with chronic kidney failure only upon receipt of a valid
prescription from a prescribing practitioner specifying or including:
(a) Documentation that the intended recipient
of the products has been trained in home dialysis therapy and will require such
products;
(b) The duration of
prescribing practitioner's order; and,
(c) The name and product code of each product
prescribed and the quantity prescribed.
(d) The prescription may indicate the person
with chronic kidney failure shall have the right to request refills of legend
drugs, devices or both, included in the schedule and described in the order for
a period of one year.
(8)
The ESRD pharmacy shall assemble the products to be delivered pursuant to the
prescribing practitioner's prescription. In assembling such products for
delivery, the ESRD pharmacy shall take steps necessary to assure the following:
(a) The code numbers and quantities of the
products assembled match the code numbers identified in the prescribing
practitioner's prescription;
(b)
With respect to any dated products, a minimum of three (3) full months of
shelf-life remain; and,
(c) All
cartons and other packaging are properly labeled as noted below:
1. "Use as Directed" statement,
2. The name and address of the person to whom
the products will be delivered,
3.
The name of the prescribing practitioner,
4. The name and address of the ESRD pharmacy
location from which the products were shipped,
5. The prescription number identifying the
shipment to the order created by the prescribing practitioner; and,
6. Any special instructions regarding
delivery dates or locations.
7. The
date after which the drug(s) and/or device(s) must be discarded.
Notwithstanding any other rule, the ESRD pharmacy may use, in lieu of a discard
after date, the manufactures expiration date when such is displayed in an
unopened sealed package.
(d) All cartons and related packaging shall
be visually inspected to confirm compliance with the specifications in
paragraph (8)(c). Compliance with the requirements set forth in paragraph
(8)(c), shall be conducted by the consulting pharmacist or independently by not
less than two employees of the ESRD pharmacy trained in the performance of the
foregoing activities, each of whom shall acknowledge in writing their
completion of such activities with respect to each group of products assembled
for delivery.
(9) The
ESRD pharmacy permit holder shall assure through visual inspection and
comparison of records that products assembled for delivery to persons with
chronic kidney failure are consistent with the prescribing practitioner's order
therefor.
(10) The products ordered
by the prescribing practitioner under this Rule shall be delivered by either
the ESRD pharmacy or a carrier authorized by the ESRD pharmacy.
(11) Upon delivery of the products by the
ESRD pharmacy or its carrier to the person identified on the prescribing
practitioner's order, the ESRD pharmacy or its carrier shall confirm receipt by
the patient or the patient's designee that the number of units delivered equals
the number of units identified on the appropriate documentation. Compliance
with the foregoing requirements set forth above shall be conducted by an
employee or agent of the ESRD pharmacy trained in the performance of such
activities, who shall acknowledge in writing the delivery of the products and
the completion of such activities with respect to each delivery.
(12) In addition to the foregoing operation
requirements, an ESRD pharmacy shall comply with the following:
(a) The ESRD pharmacy license shall be
displayed at each ESRD pharmacy location.
(b) The Board of Pharmacy shall be notified
in writing of the Consulting Pharmacist responsible, at the time of application
for the permit, for supervising the ESRD pharmacy operations and within 10
days, if the Consultant Pharmacist of record changes.
(c) The ESRD pharmacy's hours of business
shall be posted. The ESRD pharmacy shall be open such hours as are necessary to
safely and effectively dispense and deliver supplies to those persons
designated by the applicable prescribing practitioner. An ESRD pharmacy shall
provide twenty-four hour emergency and on-call service.
(d) The ESRD pharmacy shall have sufficient
space and storage capabilities as are necessary to carry out its
operation.
(e) All legend drugs
and/or legend devices included in the formulary subject to this rule shall be
properly identified.
(f) The ESRD
pharmacy shall maintain a current copy of the Florida pharmacy laws and
rules.
(g) The ESRD pharmacy shall
comply with patient counseling requirements of Rules
64B16-27.800 -.810 and
64B16-27.820,
F.A.C.
(13) ESRD Pharmacy
Application Requirements. An applicant for an ESRD pharmacy permit shall
provide the Board of Pharmacy with a Policy and Procedure Manual setting forth
in detail the operational guidelines of the applicant. The Policy and Procedure
Manual shall include a Quality Assurance Program which monitors personnel
qualifications, training and performance.
(14) An ESRD pharmacy shall be under the
control and supervision of licensed Consultant Pharmacist licensed under
Section 465.0125, F.S. The Consulting
Pharmacist shall be responsible for the drug/device delivery system.
(15) The Consultant Pharmacist of record for
the ESRD Pharmacy shall be responsible for establishing a written protocol and
Policy and Procedure Manual for the implementation of a delivery system to be
utilized in compliance with the requirements of this rule.
(16) The Consultant Pharmacist shall inspect
the permitted ESRD pharmacy on a monthly basis.
(17) A copy of the ESRD pharmacy's Policy and
Procedure Manual as provided above shall accompany the permit application,
shall be kept within the ESRD Pharmacy, and shall be available for inspection
by the Department of Health. Changes in the Policy and Procedure Manual shall
be approved by the Consulting Pharmacist.
Notes
Rulemaking Authority 465.005, 465.0125 FS. Law Implemented 465.0196, 465.022 FS.
New 10-2-94, Formerly 59X-28.850, Amended 9-20-99, 7-17-05, 6-24-08.
State regulations are updated quarterly; we currently have two versions available. Below is a comparison between our most recent version and the prior quarterly release. More comparison features will be added as we have more versions to compare.
No prior version found.