AFI41-201 MANAGING CLINICAL ENGINEERING PROGRAMS
MilReg AFI41-201 Frequently Asked Questions

What is AFI41-201 MANAGING CLINICAL ENGINEERING PROGRAMS?
AFI41-201 is an Air Force Instruction that outlines the guidelines and requirements for managing clinical engineering programs within the Air Force.

Who does AFI41-201 apply to?
AFI41-201 applies to all Air Force personnel involved in the management of clinical engineering programs, including biomedical equipment technicians, supervisors, and commanders.

What is the purpose of AFI41-201?
The purpose of AFI41-201 is to establish procedures for managing clinical engineering programs to ensure the safe and effective operation of medical equipment and systems within the Air Force.

What are the key responsibilities of clinical engineering programs?
Clinical engineering programs are responsible for acquiring, managing, maintaining, and supporting medical equipment, as well as providing technical assistance and training to medical personnel.

How are clinical engineering programs structured within the Air Force?
Clinical engineering programs are typically organized at the Medical Treatment Facility (MTF) level, under the supervision of a clinical engineering officer or biomedical equipment manager.

What are the requirements for managing medical equipment in clinical engineering programs?
Clinical engineering programs must establish a comprehensive equipment management program that includes inventory control, calibration and maintenance, equipment inspection, and incident reporting.

How is the training of biomedical equipment technicians addressed in AFI41-201?
AFI41-201 specifies that biomedical equipment technicians should receive appropriate training and certification to properly operate and maintain medical equipment within the Air Force.

Does AFI41-201 address quality assurance and safety standards for clinical engineering programs?
Yes, AFI41-201 includes provisions for quality assurance programs, safety inspections, risk management, and compliance with applicable regulations and industry standards.

What documentation and reporting requirements are outlined in AFI41-201?
AFI41-201 mandates the maintenance of equipment records, incident reports, training records, and performance metrics to ensure accountability and compliance within clinical engineering programs.

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