• There are no items in your cart

CLSI GP32 P : 1ED 2007

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

MANAGEMENT OF NONCONFORMING LABORATORY EVENTS

Superseded date

21-11-2007

Superseded by

CLSI QMS11 A : 1ED 2007

Published date

12-01-2013

Sorry this product is not available in your region.

Abstract
Committee Membership
Foreword
1 Scope
2 Definitions
3 Overview of a Nonconforming Event Management Program
4 Human Error
5 Creating a Culture to Discover and Report Nonconforming
   Events
   5.1 A Just Culture
   5.2 Nonconforming Event Management Program Support
   5.3 Detecting or Discovering Nonconforming Events
6 Initiating a Nonconforming Event Report
7 Remedial Action
   7.1 Distinction Between Remedial and Corrective Action
   7.2 Remedial Action as Corrective Action
8 Investigation
   8.1 Path of Workflow
   8.2 Investigating the Nonconformance
   8.3 Documentation of Investigation
9 Short-term Corrective Action
10 Classification
   10.1 The National Center for Patient Safety (NCPS) - Safety
         Assessment Code (SAC)
   10.2 Laboratory Event Classification
11 Analysis of Event Information and Data Presentation
   11.1 Reporting Data
   11.2 A Medical Laboratory Example
12 Management Review and Referral to Process Improvement
   for Long-term Corrective Action
   12.1 Management Review
   12.2 Root Cause Analysis
   12.3 When to Perform RCA
   12.4 Conducting an RCA
   12.5 Commonly Identified Root Causes
   12.6 Process Improvement
13 Application of Nonconforming Event Management to a
   Laboratory Example
   13.1 Initiating the Nonconforming Event Report
   13.2 Remedial Action
   13.3 Investigation - How It Happened
   13.4 Investigation - Who and What
   13.5 Investigation - Why It Happened
   13.6 Documentation of Investigation
   13.7 Short-term Corrective Action
   13.8 Classification
   13.9 Review and Referral
   13.10 Root Cause Analysis
   13.11 Process Improvement
14 Last Words of Advice
References
Additional Resources
Appendix A1. Sample of a Simple Generic Nonconforming
             Event Report
Appendix A2. Sample Laboratory Nonconforming Event Report
Appendix A3. Second Example of a Laboratory Nonconforming
             Event Report Form
Appendix A4. Example of Another Laboratory Event Management
             Form
Appendix B. The Safety Assessment Code (SAC) Matrix
Appendix C. Data Collection Tools
Appendix D. Investigation and Data Reporting Tools
Appendix E. A Formal Process for Using Root Cause Analysis
            (RCA) Tools
The Quality Management System Approach
Related CLSI/NCCLS Publications

Provides an outline and the content for developing a program to manage a healthcare service's nonconforming events that is based on the principles of quality management and patient safety.

DocumentType
Proposed Guideline
PublisherName
Clinical Laboratory Standards Institute
Status
Superseded
SupersededBy

BIS IS/ISO 15189 : 2012 MEDICAL LABORATORIES - REQUIREMENTS FOR QUALITY AND COMPETENCE
CLSI EP18 P2 : 2ED 2007 RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES

CLSI GP21 A2 : 2ED 2004 TRAINING AND COMPETENCE ASSESSMENT
CLSI HS1 A2 : 2ED 2004 A QUALITY MANAGEMENT SYSTEM MODEL FOR HEALTH CARE
CLSI GP26 A3 : 3ED 2004 APPLICATION OF A QUALITY MANAGEMENT SYSTEM MODEL FOR LABORATORY SERVICES
CLSI GP22 A2 : 2ED 2004 CONTINUOUS QUALITY IMPROVEMENT: INTEGRATING FIVE KEY QUALITY SYSTEM COMPONENTS
CLSI GP2 A5 : 5ED 2006 LABORATORY DOCUMENTS - DEVELOPMENT AND CONTROL

Access your standards online with a subscription

Features

  • Simple online access to standards, technical information and regulations.

  • Critical updates of standards and customisable alerts and notifications.

  • Multi-user online standards collection: secure, flexible and cost effective.