fda cgmp compliance 2017 - How to write error free procedures and comply with GMP regulations -By AtoZ Compliance

Key Take Away:
This cognition and human error webinar on FDA CGMP compliance will explain why it is important to understand human behavior and the psychology of error as well as to understand exactly where the instructions weaknesses are, so procedures can be human engineered, improved and/ or fixed.
Overview:
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 eliminated, many human performance problems can be prevented using GMP environmental monitoring, GMP guidelines and GMP regulations. According to human behavior experts who use human error assessment and reduction technique, human errors start at the design stage. Procedures play a vital role in human error prevention and human error reduction.
Why Should You Attend:
Procedures are very important for both execution and audits. These should be written for human factors and usability without missing important information for regulators. Usually human factors 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.
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