designing, building, and 1 maintaining a compliant sterile ... · usp history general chapter ...
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Designing, Building, and Maintaining a
Compliant Sterile Compounding Facility
Focusing on incorporating USP <800> Requirements
1
NCHEA Spring SeminarMarch 2018
Presented by Leach Wallace Associates, Inc.
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Outline of discussion
Brief Introduction of Standards USP <800> Planning & Project Development Design requirements ArchitecturalMEP Design exampleConsiderations for Management
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USP Compounding Compendium USP <795>, <797>, and <800>
Standards for preparing compounded sterile drugs to ensure patient safety
<795> Nonsterile drugs <797> Sterile drugs
Standards for safe handling of hazardous drugs to focus on worker safety
<800> Hazardous drugs
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Current Status USP <797> latest release which is
enforceable was made official on June 1, 2008.
Significant comments were received on the first release of a proposed revision for public comments during the Sept 2015 to Jan 2016 review.
Revision to USP <797> is due to be published in Sept/Oct 2018 for second round of public comment.
USP <800> was postponed to align with the next official release date of USP <797>.
Anticipated to become “official” December 1, 2019
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USP <797> Changes with Engineering Controls Removal of references to Hazardous
Drugs Defined Temperature & Relative
Humidity Requirements20°C (68°F) or cooler< 60% RH
No in-room humidifiers or de-humidifiers Defined interval for Environmental
Monitoring- Monthly
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USP <800> Hazardous Drugs in Healthcare Settings
Purpose-describe practice and quality standards for handling hazardous drugs in healthcare settings
Patient safetyWorker safety Environmental
protection
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USP<800> HistoryGeneral Chapter <800> History- Part of USP<797> 2004, 2008March 2014- 1st revision published for
commentOctober 2015- 2nd revision published
for commentOriginal expected date of recognition
was February 1, 2016 Official- grace period.
Each State Board of Pharmacy will determine effective date-TBD
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Areas of coverage
Product transport StorageCompounding Preparation Administration
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Where does it apply?
All healthcare personnel that handle HD preparations
Pharmacies HospitalsOther healthcare institutionsCancer centers Patient treatment clinics Physicians practice facilities
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Enforcement
State Pharmacy boards State Regulators FDAOther government authorities JHACO
USP does not enforce standards
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Overall Regulatory TrendsExpectation of existing facility
improvementsDocumented State of Control verified
by dataBoards of Pharmacy want self
reporting of adverse events Regulators expecting compliance–
Pharmacies tasked with creation/maintenance of Quality Program to maintain compliance (FDA like mentality).
USP chapters on compounding are federally recognized as the standard of practice in the U.S.
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Planning & Project Development 12
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Planning and Project Development
Assembling the team Determine project
scope and goals Review
considerations Program
development Design
ConstructionCommissioning Testing and
CertificationMaintenance of
facilityCompliance
model
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Assembling the team
Pharmacy staff Pharmacy
Consultant Safety Officer Infection Control Facilities
EVS Administration Architect EngineerOthers…..
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Determine project scope and goals ProceduresMaintainabilityCost/Budget Standard operating modes Emergency plansCertification StandardCompliance methodology Environment Expectations vs results
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Challenges/Considerations Square footage requirements and
thorough analysis of personnel and material workflows critical in design/re-design process
Renovation vs. New Construction Dedicated Exhaust and/or HVAC Systems Back Up Power Temperature/Relative Humidity
requirements Pressurization Detailed understanding/completion of
SOPs prior to facility completion- cleaning, EM
Commissioning/As-Built verification
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Other Considerations
Risk assessmentPersonnel trainingPersonal Protective
Equipment (PPE) Facilities and
Engineering ControlsEnvironmental Quality
and Control –Environmental monitoring(lab spaces, break rooms, retail space)
Medical Surveillance
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Design Requirements18
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Temperature and humidityPositive pressureNegative pressure (Hazardous
Drugs)Air changesCleanable surfacesSealed wall and ceiling juncturesAppropriate equipment and
essential activities only
19 Facility Requirements-Design
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Facility Requirements-Equipment C-SEC – Containment Secondary Engineering
Control Room envelope that maintains negative
pressure with appropriate air changes C -PEC - Containment Primary Engineering
Control Hood or Cabinet
Hood and HEPA filter certification at 6 month intervals
Calibration SOPs Documentation
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Facility Requirements-Cleaning
Specifies procedures for routine cleaning, decontamination, deactivation and disinfection of the room(s) and Containment-Primary Engineering Controls (C-PEC)/Hoods.
Details location of dedicated cleaning equipment- no mop sinks!
If EVS closet is located off anteroom-pressure monitor is highly recommended
Must be considered when selecting floor and millwork finishes
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Environmental Quality & Control
Air QualityDifferential PressureSurface Testing Temperature and HumidityAction and Alert limits
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Example: Monitoring of Temperature and Humidity Manual: Hygrometer daily logging on chart.
Data logger.
Continuous monitoring through ATC system.
Setpoints
Alarm points
Trend data
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What happens if the design temperature is 68 degrees and the temperature sensor says 68.2 degrees?
“These facilities shall also provide a comfortable and well lighted working environment, which typically includes a temperature of 20 degrees(68 degrees F) or cooler, to maintain comfortable conditions for compounding personnel to perform flawlessly when attired in the required aseptic compounding garb.”
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Is it due to sensor calibration? Duration of temperature differential?Causes of temperature differential? Alarm? Action? Report per Quality Control Plan?
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Architectural Considerations26
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USP <800> Facility Design
Restricted accessUnpackingStorageSpillsNon sterile
and sterile compounding
No Positive Pressure Areas for Hazardous Drugs
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USP <800> Facility Requirements
Compounding areas away from breakrooms, refreshment areas, staff, patients, or visitors.
SEPARATE designated areas shall be available for: Unpacking HDs* Non sterile HD Compounding Sterile HD Compounding Storing HDs (unless buffer area is used)
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USP <800> Storage
• Storage (unpacking) room must be negative pressure, 12 ACH, and vented outside.
• Cannot store on floors.• HDs stored in manner to prevent
breakage or spillage• Substantial challenge for most
pharmacy floor plans.• Specified PPE
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Hazard Communication Program
Required by OSHA Employers required to establish
policies and procedures to ensure worker safety in all aspects of distribution of drugs as part of OSHA Hazardous Communication Standard (HCS)
Specifies PPE for each activity associated with receiving, handling, stocking, compounding, administering, clean up, and spill remediation.
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Cleaning Specifies procedures for routine
cleaning, decontamination, deactivation and disinfection of the room(s) and Containment-Primary Engineering Controls (C-PEC).
References Cleaning Section of USP <797>
Specifies PPEMust be considered when
selecting floor and millwork finishes
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USP <800> Challenges/Considerations
Square footage requirements and thorough analysis of personnel and material workflows critical in design/re-design process
Renovation vs. new construction Dedicated Exhaust and/or Air Handling Systems Temp/RH Segregated Storage in its own room External venting- hoods/rooms Differential Pressure requirements Detailed understanding/completion of SOPs
prior to facility completion- cleaning, EM Commissioning/As-Built verification
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Architectural Considerations Prefabricated clean rooms vs site build
out Seamless Flooring Drywall Ceilings
Eliminate or minimize access panels Door Sweeps/Seals Pass-Throughs (Sealed) Sink Locations Eyewash Locations Powered Door Operators
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MEP Considerations34
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Electrical Design Requirements
Emergency PowerCritical or Equipment branch
HEPA Fan-Powered Filter ModulesChemo HoodChemo Hood Exhaust FanUSP <800> Room Exhaust FanRoom Pressure MonitorsSealed Lighting FixturesRefrigeratorsSecurity System devicesPharmacy equipment
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General Pharmacy Design Criteria 4 Air changes per hour 2 Outside air changes per hour Positive pressurization Negative pressurization (HD
areas) Temperature 65°-70°F RH < 60%
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HVAC Design Options
ISO 7 Clean RoomCompounding within an ISO 5/
Class 100 Clean RoomRoom Air Change RequirementsProvide “House” airflow for
cooling loads and pressurization requirements
Air Change Requirements provided by ceiling-mounted fan-powered HEPA modules
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Room Air Change Rates and Filtration Requirements
VELOCITY & AIR CHANGE RATES FOR SELECTED CLEAN SPACE CLASSESSpace Classification Average Room
Velocity (fpm)Air Changes
per HourFiltered Ceiling
CoverageISO Federal Standard 209E
5 100 40-80 240-480 100%7 10,000 10-15 30-60 5-40%8 100,000 1-8 5-30 --
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Facility Requirements-Air ISO Guidelines for clean
areas must be met ISO Class 5 Laminar Flow
Hoods or BSCs ISO Class 7 for Buffer
Area/Cleanroom ISO Class 8 for Anteroom
(non-hazardous drugs) ISO Class 7 for Anteroom
(hazardous drugs)
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Airflow Summary40
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Cooling Loads
Cooling Load Calculations Room Envelope
WallsRoof Load
Internal LoadsPeopleLighting EquipmentHood(s)
Heat Gain from Fan-Powered HEPA Module FansConsider Source
System 24/7/365 Typical Outpatient Facility HVAC systems
operate on occupied/unoccupied modes
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HVAC Systems: Air Handling Systems
Typical In-Hospital Systems Operate 24/7/365 Higher Percentages of Outdoor Air
To accommodate Chemo Hood and Unpacking Room makeup air requirements
Reheat Systems60% Maximum humidity threshold
ok with 68°F Room Temperature
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HVAC Systems: Air Handling Systems
Typical Outpatient Facility Systems DX (Direct Expansion)Rooftop Units Designed for minimum outdoor air Additional features/controls are needed to
maintain maximum 60% space humidity due to increased outdoor airDigital scroll compressor(s) for capacity
controlHot gas reheat/ dehumidification controls
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Example Pharmacy45
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Airflow Schematic I49
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Airflow Schematic II51
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Airflow Schematic III52
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Summary for Management Consideration
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Key Questions for Pharmacy Management
Does our facility meet requirements? Do our personnel and material workflows
work with or against our specific facility and engineering controls?
Do we have a documented state of control? Do we identify, investigate, correct and
document adverse environmental events? Does the C-Suite understand the risk
associated with non-compliance? What is our compliance budget/resources?Can small satellite/oncology practices afford
compliance?
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Questions ?
Ken Frazier, PE Leach Wallace Associates, Inc., [email protected], 704-335-0485, 410-579-8100
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