22 Tex. Admin. Code § 291.94 - Records
(a) Maintenance of records.
(1) Every inventory or other record required
to be kept under the provisions of §
291.91 of this title (relating to
Definitions), §
291.92 of this title (relating to
Personnel), §
291.93 of this title (relating to
Operational Standards), and §
291.94 of this title (relating to
Records), contained in Clinic Pharmacy (Class D) shall be:
(A) kept by the pharmacy and be available,
for at least two years from the date of such inventory or record, for
inspecting and copying by the board or its representative and to other
authorized local, state, or federal law enforcement agencies; and
(B) supplied by the pharmacy within 72 hours,
if requested by an authorized agent of the Texas State Board of Pharmacy. If
the pharmacy maintains the records in an electronic format, the requested
records must be provided in a mutually agreeable electronic format if
specifically requested by the board or its representative. Failure to provide
the records set out in this section, either on site or within 72 hours,
constitutes prima facie evidence of failure to keep and maintain records in
violation of the Act.
(2) Records, except when specifically
required to be maintained in original or hard-copy form, may be maintained in
an alternative data retention system, such as a data processing system or
direct imaging system provided:
(A) the
records maintained in the alternative system contain all of the information
required on the manual record; and
(B) the data processing system is capable of
producing a hard copy of the record upon the request of the board, its
representative, or other authorized local, state, or federal law enforcement or
regulatory agencies.
(3)
Invoices and records of receipt may be kept at a location other than the
pharmacy. Any such records not kept at the pharmacy shall be supplied by the
pharmacy within 72 hours, if requested by an authorized agent of the Texas
State Board of Pharmacy.
(b) On-site visits. A record of on-site
visits by the pharmacist-in-charge, consultant pharmacist, or staff pharmacist
shall be maintained and include the following information:
(1) date of the visit;
(2) pharmacist's evaluation of findings;
and
(3) signature of the visiting
pharmacist.
(c)
Prepackaging. Records of prepackaging shall include the following:
(1) name, strength, and dosage form of
drug;
(2) name of the
manufacturer;
(3) manufacturer's
lot number;
(4) expiration
date;
(5) facility's lot
number;
(6) quantity per package
and number of packages;
(7) date
packaged;
(8) name(s), signatures,
or electronic signatures of the supportive personnel who prepackages the drug
under direct supervision of a pharmacist; and
(9) name, signature, or electronic signature
of the pharmacist who prepackages the drug or supervises the prepackaging and
checks and releases the drug.
(d) Labeling. Records of labeling of drugs or
devices in original manufacturer's containers shall include the following:
(1) name and strength of the drug or device
labeled;
(2) name of the
manufacturer;
(3) manufacturer's
lot number;
(4) manufacturer's
expiration date;
(5) quantity per
package and number of packages;
(6)
date labeled;
(7) name of the
supportive personnel affixing the label; and
(8) the signature of the pharmacist who
checks and releases the drug.
(e) Provision. Records of drugs and/or
devices provided shall include logs, patient records, or other acceptable
methods for documentation. Documentation shall include:
(1) patient name;
(2) name, signature, or electronic signature
of the person who provides the drug or device;
(3) date provided; and
(4) the name of the drug or device and
quantity provided.
(f)
Dispensing. Record-keeping requirements for dangerous drugs dispensed by a
pharmacist are the same as for a Class A pharmacy as set out in §
291.34 of this title (relating to
Records).
Notes
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