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Medical Professional CHFM Exam Syllabus Topics:

SectionWeightObjectives
Topic 1: Planning, Design and Construction18%- Capital project planning and management
- Infection control and risk assessment
- Interim life safety measures
- Construction safety and commissioning
Topic 2: Maintenance and Operations27%- Utilities and operational continuity
- Preventive maintenance and asset management
- Medical gas and emergency power systems
- Building systems: HVAC, electrical, plumbing
Topic 3: Finance Management10%- Cost control and financial reporting
- Life-cycle cost analysis
- Operating and capital budgeting
- Deferred maintenance and stewardship
Topic 4: Compliance33%- Emergency preparedness and response
- Life safety and fire safety
- Documentation, inspections and corrective actions
- Regulatory standards and codes
Topic 5: Administration12%- Leadership and organizational management
- Strategic and performance management
- Workforce development and safety programs
- Policies, procedures and communication

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Medical Professional Certified Healthcare Facility Manager (CHFM) certification exam Sample Questions (Q109-Q114):

NEW QUESTION # 109
The initial cost of installing a building automation system is primarily a function of the

Answer: C

Explanation:
Building automation system (BAS) costs are based largely on the number of control points (sensors, outputs, and monitored parameters) that must be integrated. The cost is driven by how many signals must be tracked, rather than just the square footage or vendor.
A: Gross square footage can influence scope, but cost scales with monitored points.
B: Vendor may affect pricing, but primary cost driver is point count.
C: Technology choice matters, but the quantity of control points is more significant.
Reference: ASHE/AHA CHFM study materials - Planning, Design, and Construction.


NEW QUESTION # 110
A measured carbon dioxide level of 1,500 ppm in an area of a facility may indicate

Answer: D

Explanation:
Acceptable indoor CO# concentrations in healthcare facilities are generally expected to remain below 1,000 ppm, as recommended by ASHRAE Standard 62.1 (Ventilation for Acceptable Indoor Air Quality). A reading of 1,500 ppm typically signals inadequate ventilation and insufficient outside air being introduced into the space. This is a direct indicator of poor dilution of indoor contaminants.
Correct: Lack of outside air (C) - High CO# concentrations are directly linked to reduced outside air supply.
Incorrect:
A). Within design - Not correct, since 1,500 ppm exceeds design thresholds.
B). Vehicular exhaust - Would raise CO and NOx levels, not primarily CO#.
D). Humidity/dewpoint - Unrelated to CO# measurement.
References:
ASHRAE 62.1: Ventilation for Acceptable Indoor Air Quality.
CHFM Candidate Handbook - Maintenance and Operations domain: ventilation standards.
________________________________________


NEW QUESTION # 111
Construction and/or renovation project submittals and shop drawings are reviewed to ensure

Answer: D

Explanation:
Submittals and shop drawings are specifically reviewed to ensure compliance with the design intent, plans, and specifications prepared by the architect/engineer. Code compliance is established during design and permitting, while minimizing change orders or ensuring contractor understanding are indirect benefits.
References: AIA A201 General Conditions; AHA/ASHE CHFM Handbook - Planning, Design, and Construction domain.


NEW QUESTION # 112
The Safe Medical Device Act of 1990 requires reporting of incidents involving a medical device when which of the following occurs?

Answer: C

Explanation:
The Safe Medical Device Act (SMDA) of 1990 requires healthcare facilities to report to the FDA and the manufacturer when a device is suspected of causing or contributing to death or serious injury.
C). death or injury (Correct): Specifically mandated under SMDA.
A). inappropriate application: A usage issue, not a reporting trigger.
B). recall: Issued by the FDA/manufacturer, not the facility's reporting obligation.
D). major breakdown: Requires service but not mandatory reporting.
References:
Safe Medical Device Act of 1990, Public Law 101-629.
FDA Medical Device Reporting (MDR) requirements.
CHFM Candidate Handbook - Compliance domain.
________________________________________


NEW QUESTION # 113
Which of the following is required for airborne infection isolation rooms?

Answer: D

Explanation:
Per CDC Guidelines and ASHRAE/FGI requirements adopted into NFPA 99, airborne infection isolation (AII) rooms must maintain negative pressure relative to adjacent areas and provide a visual pressure monitoring mechanism (e.g., manometer, electronic monitor).
A: HEPA/UV is supplemental, not a universal requirement.
B: Minimum is 12 air changes per hour, not 20.
C: Anterooms may be provided but are not universally required.
References: CDC, Guidelines for Environmental Infection Control in Health-Care Facilities; FGI Guidelines for Design and Construction of Hospitals; NFPA 99.


NEW QUESTION # 114
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