1.
Access to the animal facility is limited or restricted at the
discretion of the laboratory or animal facility director.
2.
Personnel wash their hands after handling cultures and animals,
after removing gloves, and before leaving the animal facility.
3.
Eating, drinking, smoking, handling contact lenses, applying cosmetics,
and storing food for human use are not permitted in animal rooms.
Persons who wear contact lenses in animal rooms should also wear
goggles or a face shield.
4.
All procedures are carefully performed to minimize the creation
of aerosols.
5.
Work surfaces are decontaminated after use or after any spill
of viable materials.
6.
Doors to animal rooms open inward, are self-closing and are kept
closed when experimental animals are present.
7.
All wastes from the animal room are appropriately decontaminated,
preferably by autoclaving, before disposal. Infected animal carcasses
are incinerated after being transported from the animal room in
leakproof, covered containers.
8.
An insect and rodent control program is in effect.
1.
The laboratory or animal facility director limits access to the
animal room to personnel who have been advised of the potential
hazard and who need to enter the room for program or service purposes
when work is in progress. In general, persons who may be at increased
risk of acquiring infection, or for whom infection might be unusually
hazardous, are not allowed in the animal room.
2.
The laboratory or animal facility director establishes policies
and procedures whereby only persons who have been advised of the
potential hazard and meet any specific requirements (e.g., immunization)
may enter the animal room.
3.
When the infectious agent(s) in use in the animal room requires
special entry provisions (e.g., the need for immunizations and
respirators) a hazard warning sign, incorporating the universal
biohazard symbol, is posted on the access door to the animal room.
The hazard warning sign identifies the infectious agent(s) in
use, lists the name and telephone number of the animal facility
supervisor or other responsible person(s), and indicates the special
requirement(s) for entering the animal room.
4.
Laboratory personnel receive appropriate immunizations or tests
for the agents handled or potentially present in the laboratory
(e.g., hepatitis B vaccine or TB skin testing).
5.
When appropriate, considering the agents handled, baseline serum
samples from animal care and other at-risk personnel are collected
and stored. Additional serum samples may be collected periodically
depending on the agents handled or the function of the facility.
The decision to establish a serologic surveillance program must
take into account the availability of methods for the assessment
of antibody to the agent(s) of concern. The program should provide
for the testing of serum samples at each collection interval and
the communication of results to the participants.
6.
A biosafety manual is prepared or adopted. Personnel are advised
of special hazards, and are required to read and to follow instructions
on practices and procedures.
7.
Laboratory personnel receive appropriate training on the potential
hazards associated with the work involved, the necessary precautions
to prevent exposures, and the exposure evaluation procedures.
Personnel receive annual updates, or additional training as necessary
for procedural or policy changes.
8.
A high degree of precaution must always be taken with any contaminated
sharp items, including needles and syringes, slides, pipettes,
capillary tubes, and scalpels. Needles and syringes or other sharp
instruments are restricted in the animal facility for use only
when there is no alternative, such as for parenteral injection,
blood collection, or aspiration of fluids from laboratory animals
and diaphragm bottles. Plasticware should be substituted for glassware
whenever possible.
a.
Only needle-locking syringes or disposable syringe-needle units
(i.e., needle is integral to the syringe) are used for injection
or aspiration of infectious materials. Used disposable needles
must not be bent, sheared, broken, recapped, removed from disposable
syringes, or otherwise manipulated by hand before disposal;
rather, they must be carefully placed in conveniently located
puncture-resistant containers used for sharps disposal. Non-disposable
sharps must be placed in a hard-walled container for transport
to a processing area for decontamination, preferably by autoclaving.
b.
Syringes which re-sheathe the needle, needle-less systems, and
other safe devices should be used when appropriate.
c.
Broken glassware must not be handled directly by hand, but must
be removed by mechanical means such as a brush and dustpan,
tongs, or forceps. Containers of contaminated needles, sharp
equipment, and broken glass should be decontaminated before
disposal, according to any local, state, or federal regulations.
9.
Cultures, tissues, or specimens of body fluids are placed in a
container that prevents leakage during collection, handling, processing,
storage, transport, or shipping.
10.
Cages are appropriately decontaminated, preferably by autoclaving,
before they are cleaned and washed. Equipment and work surfaces
should be decontaminated with an appropriate disinfectant on a
routine basis, after work with infectious materials is finished,
and especially after overt spills, splashes, or other contamination
by infectious materials. Contaminated equipment must be decontaminated
according to any local, state, or federal regulations before it
is sent for repair or maintenance or packaged for transport in
accordance with applicable local, state, or federal regulations,
before removal from the facility.
11.
Spills and accidents which result in overt exposures to infectious
materials are immediately reported to the laboratory director.
Medical evaluation, surveillance, and treatment are provided as
appropriate and written records are maintained.
12.
Animals not involved in the work being performed are not permitted
in the lab.