Bookmark Add to Calendar

How to Write Procedures to Avoid Human Errors

Duration : 90 Minutes

Ginette Collazo, PH.D,

Ginette Collazo, Ph. D. is an Industrial-Organizational Psychologist with 20 years of experience that specializes in Engineering Psychology and Human Reliability, disciplines that study the interaction between human behavior and productivity. She has held positions leading training and human relia Read more


Human error is known to be the major cause of quality and production losses in many industries. Although it is unlikely that human error will ever be totally eliminated, many human performance problems can be prevented. Human errors start at the design stage. Procedures play a vital role in human reliability. Nevertheless, it is really important to understand human behavior and the psychology of error as well as understand exactly where the instructions weaknesses are, so procedures can be human engineered, improved and/or fixed.

Course Objective:

Procedures are very important for both execution and audits. These should be written for users without missing important information for regulators. Usually procedures have weaknesses that harm productivity, quality and regulatory standing. We will discuss from content development to formats designed for human error reduction due to procedures.

Course Outline:

• SOP writing outline
• Content development
• The rational for procedure use
• Regulatory compliance background
• Universal purpose of procedures
• The Human perspective
• Human Error as a root cause
• The thinking and reading process
• Common mistakes and causes
• How to create and maintain a procedure
• Goals of a procedure
• Good Procedure Writing practices (Terminology, Formats, layouts, mixed cases, steps content, common words, references, branching, conditional steps, the use of “Precautions”, “Warnings” and “Cautions”,
• Procedure styles
• Use of electronic information networks for procedure access

What You Get:

•  Training Reference Materials
•  SOP Template
•  Live Q&A with our Expert
•  Participation Certificate
•  Access to Signup Community (Optional)
•  Reward Points

Who Will Benefit:

• QA/QC directors and managers
• Process improvement/excellence professionals
• Training directors and managers
• Plant engineering
• Compliance officers
• Regulatory professionals
• Executive management
• Manufacturing operations directors
• Human factors professionals

Please reach us at 1-888-844-8963 for any further assistance or if you wish to register

Contact Us



Similar Trainings

Best Practices for Purchasing and Supplier Controls in the Medical Device Industry
LIVE : Scheduled on 11-December-2020 :01:00 PM EST
How to Prepare For and Host a FDA Inspection and Respond to 483’s
LIVE : Scheduled on 11-January-2021 :01:00 PM EST
Understanding ISO 13485 and its Relation to FDA's Quality Systems Regulation
LIVE : Scheduled on 15-January-2021 :01:00 PM EST
paypal payment Comodo

Copyright ©2020 Grey Compliance. All rights reserved. | DBA Signuptraining.com