Mich. Admin. Code R. 338.3510 - Animal euthanasia; retention of records regarding receipt and administration of sodium pentobarbital and animal tranquilizers
Rule 10.
(1) The
permit holder shall maintain separate records of the receipt of commercially
prepared, pre-mixed solution of sodium pentobarbital and animal tranquilizers
and the administration of a commercially prepared, pre-mixed solution of sodium
pentobarbital and animal tranquilizers at the animal control shelter, animal
protection shelter, or by the class B dealer.
(2) These records must include all of the
following information pertaining to the receipt of commercially prepared,
pre-mixed solution of sodium pentobarbital and animal tranquilizers:
(a) The date of acquisition.
(b) The quantity acquired.
(c) The name of the drug.
(d) The trade name of the drug.
(e) The lot number and strength of a
commercially prepared, pre-mixed solution of sodium pentobarbital or animal
tranquilizer.
(3) The
records of the administration of the commercially prepared, pre-mixed solution
of sodium pentobarbital or animal tranquilizer for the purpose of practicing
euthanasia, must include all of the following:
(a) The quantity used.
(b) The time and date it was
administered.
(c) The name of the
individual who administered the animal tranquilizer or pre-mixed solution of
sodium pentobarbital.
(d) The full
description of the animal to which the commercially prepared, pre-mixed
solution of sodium pentobarbital or animal tranquilizer was administered, which
includes all of the following and is recorded in the animal's medical or
shelter record:
(i) The species of the
animal.
(ii) The breed of the
animal.
(iii) The sex of the
animal.
(iv) The age of the
animal.
(v) The approximate weight
of the animal.
(vi) The number
associated with the animal if a numbering system is used.
(4) The permit holder shall record
receipt of controlled substances on DOJ DEA order forms pursuant to 21 CFR part
1305 (2019). 21 CFR part 1305 is available at no cost on the internet at
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=1305.
Printed copies of 21 CFR part 1305 are available for inspection and
distribution at 10 cents per page from the Michigan Board of Pharmacy,
Department of Licensing and Regulatory Affairs, Bureau of Professional
Licensing, 611 West Ottawa, P.O. Box 30670, Lansing, Michigan 48909.
(5) The permit holder shall maintain records
of administration of controlled substances pursuant to 21 CFR part 1304 (2019).
21 CFR part 1304 is available at no cost on the internet at
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=1304.
Printed copies of 21 CFR part 1304 also are available for inspection and
distribution to the public at 10 cents per page from the Michigan Board of
Pharmacy, the Department of Licensing and Regulatory Affairs, Bureau of
Professional Licensing, 611 West Ottawa, P.O. Box 30670, Lansing, Michigan
48909.
(6) Permit holders shall
keep records for a period of 2 years and shall make them available for
inspection by the department or other authorized individual upon
request.
Notes
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