Wash. Admin. Code § 296-62-50025 - Engineering controls
(1) Evaluate and
implement appropriate engineering controls to eliminate or minimize employee
exposure. Examples of engineering controls include, but are not limited to:
(a) Closed system transfer devices.
(b) Safer sharps devices.
(c) Safety interlocks.
(d) Ventilated cabinets.
(2) Ventilated cabinets.
(a) Prepare (e.g., mix, compound, crush)
hazardous drugs inside an appropriate ventilated cabinet or barrier isolators
designed to prevent worker exposure.
(i)
Alternate precautions may be used where the hazard assessment determines a low
occupational exposure risk while preparing hazardous drugs other than
chemotherapy agents (e.g., crushing and splitting tablets, drawing medication
into a syringe). These may include, but are not limited to, temporarily
designating a preparation area, use of appropriate personal protective
equipment, and instituting cleaning procedures.
(ii) Chemotherapy drugs must be prepared in
an appropriate ventilated cabinet with the exception of circumstances where the
employer can document evidence of a clinical need (e.g., there is a nonroutine
need to provide chemotherapy treatment, compounding services are not readily
available, and it is in the best interest of the patient to provide local
care). In such circumstances alternate precautions must be instituted as
described above.
(b)
Hazardous drugs that volatilize must be handled only in a ventilated cabinet
that captures the volatilized material to prevent employee exposure, or in a
ventilated cabinet that does not recirculate air inside the cabinet or exhausts
air back into the room environment.
(c) Install and maintain the ventilation
equipment determined by your hazard assessment in accordance with:
(i) The ventilation equipment manufacturer's
design, instructions, and precautions;
(ii) Appropriate and most current national
safety and industry standards.
| Note: | The following are examples of industry standards related to installing and maintaining ventilation equipment. There may be other industry standards in addition to those listed below: |
(A) Center for
Disease Control/National Institute for Health: Primary Containment for
Biohazards: Selection, Installation and Use of Biological Safety Cabinets (CDC/
NIH).
(B) National Sanitation
Foundation/American National Standards Institute Standard 49, (NSF/ANSI) Class
II (laminar flow) Biosafety Cabinetry.
(C) U.S. Pharmacopeial Convention
(USP).
(D) American Glove Box
Standards.
(iii)
National Institute of Occupational Safety and Health (NIOSH) "Preventing
Occupational Exposure to Antineoplastic and Other Hazardous Drugs in Health
Care Settings"; and
(iv) Applicable
state, federal, and local regulations.
(d) Develop and implement maintenance and
cleaning procedures that ensure the effectiveness and safety of the ventilated
cabinet.
(i) Field-certify biosafety cabinet
performance, in accordance with National Sanitation Foundation/American
National Standards Institute Standard 49, after installation, relocation,
maintenance, repairs to internal components, HEPA filter replacement, and every
six months thereafter or as recommended by the manufacturer.
(ii) Select appropriate performance and test
methods for isolators, depending on the type (containment only or aseptic
containment), the operating pressure (positive or negative and designed
magnitude), and toxicity of the hazardous drug. At a minimum, conduct leak and
containment integrity tests in accordance with current American Glovebox
Society guidelines. In addition perform a HEPA filter leak test for those
isolators that utilize HEPA filtration.
(iii) Prominently display a current
field-certification label on the ventilated cabinet.
(iv) Make sure that workers performing
maintenance are familiar with applicable safety procedures, warned about
hazards (e.g., through the provision of material safety data sheet or other
equivalent information resources), and trained in appropriate work techniques
and PPE needed to minimize exposure.
(v) Remove all hazardous drugs and chemicals,
and decontaminate the ventilated cabinet before beginning maintenance
activities.
(vi) Notify occupants
in the affected areas immediately before the maintenance activity begins, and
place warning signs on all affected equipment.
(vii) Deenergize the ventilated cabinet in
accordance with chapter 296-803 WAC, Lockout/Tagout (control of hazardous
energy).
(viii) Decontaminate and
bag equipment parts removed for replacement or repair before they are taken
outside the facility.
(ix) Seal
used filtration media in plastic immediately upon removal, and dispose as
contaminated waste.
| Note: | Consult the following documents for performance test methods and selection criteria for ventilated cabinets: |
| (1) Primary Containment for Biohazards: Selection, Installation and Use of Biological Safety Cabinets (CDC/NIH). | |
| (2) NSF/ANSI 49, Class II (laminar flow) Biosafety Cabinetry. |
Notes
Statutory Authority: RCW 49.17.010, 49.17.040, 49.17.050, 49.17.060, and 2011 c 39. 12-02-053, § 296-62-50025, filed 1/3/12, effective 1/1/14 and (2) effective 1/1/15.
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