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Failure Mode and Effects Analysis for Joint Commission Requirements - By Compliance Global Inc
This Webinar is over
Date | Mar 26, 2015 |
Time | 01:00 PM EDT |
Cost | $145.00 |
Online
|
Overview:
Failure mode and effects analysis (FMEA) is one method hospitals can use to comply with the requirement by the Joint Commission on Accreditation of Healthcare Organizations (JCAHO) that they conduct at least one proactive risk assessment of a high-risk process each year.
While it is not the only means of satisfying the requirement,Failure Mode Effect Analysis is used to assess the efficacy and efficiency of medical devices.
Why Should You Attend:
FMEA is an established and widely used procedure in almost all industries including healthcare. FMEA is not, however, a simple procedure.
It is of immense use for the high-risk processes such as programming infusion pumps for intravenous delivery of medications, surgical robots, diagnosing a disease, and performing ER interventions. The entire team has to grasp the fundamentals from start to finish because a cross-functional brainstorming is a requirement.
Areas Covered in the Session:
The Joint Commission regulations
FMEA process
Preparation for FMEA
Variations in FMEAs
Team selection and guidance
Improving team efficiency
Identifying failure modes
Identifying system-wide causes
Severity rating
Frequency rating
Detection rating
Risk mitigation
FMEA verification
FMEA procedure at VA hospitals
Examples at other hospitals
Learning Objectives:
You will :
Learn to eliminate and minimize risks
Understand the principles of designing a robust process for patient care
Learn to simplify and standardize a procedure
Learn how to prevent harm to patients
Who Will Benefit:
Senior management
All doctors
All nurses
Quality assurance staff
Patient safety staff
Risk managers
Hospital administrators
Level:
Beginner
For more detail please click on this below link
https://www.complianceglobal.us/product/700028
Failure mode and effects analysis (FMEA) is one method hospitals can use to comply with the requirement by the Joint Commission on Accreditation of Healthcare Organizations (JCAHO) that they conduct at least one proactive risk assessment of a high-risk process each year.
While it is not the only means of satisfying the requirement,Failure Mode Effect Analysis is used to assess the efficacy and efficiency of medical devices.
Why Should You Attend:
FMEA is an established and widely used procedure in almost all industries including healthcare. FMEA is not, however, a simple procedure.
It is of immense use for the high-risk processes such as programming infusion pumps for intravenous delivery of medications, surgical robots, diagnosing a disease, and performing ER interventions. The entire team has to grasp the fundamentals from start to finish because a cross-functional brainstorming is a requirement.
Areas Covered in the Session:
The Joint Commission regulations
FMEA process
Preparation for FMEA
Variations in FMEAs
Team selection and guidance
Improving team efficiency
Identifying failure modes
Identifying system-wide causes
Severity rating
Frequency rating
Detection rating
Risk mitigation
FMEA verification
FMEA procedure at VA hospitals
Examples at other hospitals
Learning Objectives:
You will :
Learn to eliminate and minimize risks
Understand the principles of designing a robust process for patient care
Learn to simplify and standardize a procedure
Learn how to prevent harm to patients
Who Will Benefit:
Senior management
All doctors
All nurses
Quality assurance staff
Patient safety staff
Risk managers
Hospital administrators
Level:
Beginner
For more detail please click on this below link
https://www.complianceglobal.us/product/700028
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