CBA Healthcare Facility Operations & Safety Standards Flashcards
6 cards from real CBA practice questions. Tap to flip, then mark Knew It or Still Learning — missed cards come back until you master them.
Read the first 6 CBA Healthcare Facility Operations & Safety Standards flashcards as text
The Joint Commission's tracer methodology during accreditation surveys is BEST described as:
Answer: Following an individual patient's care experience to evaluate system compliance across departments
Tracer methodology follows a specific patient's care journey across departments, revealing how well interconnected systems—including biomedical equipment management—function in practice.
A hospital's infection control risk assessment (ICRA) is most relevant to a biomedical auditor when:
Answer: Planning construction or renovation activities near clinical areas that may affect medical equipment
The ICRA evaluates infection risks from construction or renovation activities, which can directly affect nearby medical equipment and require biomedical involvement in risk mitigation.
OSHA's Bloodborne Pathogens Standard (29 CFR 1910.1030) is relevant to biomedical technicians because:
Answer: It mandates exposure control plans for workers who may contact blood or other potentially infectious materials during device servicing
Biomedical technicians servicing equipment contaminated with blood or body fluids are covered by OSHA's Bloodborne Pathogens Standard, requiring exposure control plans, PPE, and training.
Which document is REQUIRED by The Joint Commission to demonstrate that a healthcare organization has evaluated and managed utility system risks?
Answer: A utility systems management plan
TJC's Environment of Care standards require a written utility systems management plan that identifies risks and defines maintenance strategies for critical building systems.
The FDA's Medical Device Reporting (MDR) regulation (21 CFR Part 803) requires hospitals to report device-related adverse events when:
Answer: A device malfunction could cause or contribute to serious injury or death if it were to recur
21 CFR Part 803 requires user facilities (hospitals) to report device malfunctions to FDA when recurrence of the malfunction could cause or contribute to serious injury or death.
A biomedical auditor evaluating a hospital's hazardous waste management program for biomedical-related waste should reference:
Answer: RCRA regulations (EPA 40 CFR Parts 260-268) and state environmental regulations
Hazardous waste generated by biomedical activities (solvents, batteries, fluorescent bulbs) is regulated under RCRA by the EPA, with additional state-level requirements.