Two Day Seminar: How to Write Error Free Procedures and Comply with GMP Regulations (Tampa, FL, United States - October 19th-20th, 2017) - Research and Markets

DUBLIN--()--Research and Markets has announced the addition of the "How to Write Error Free Procedures and Comply with GMP Regulations" conference to their offering.

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.

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.

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.

Areas Covered In the Seminar:

- SOP writing outline

- Content development

- The rational for procedure use

- Regulatory compliance background

- Universal purpose of procedures

- Background on Human Error Phenomena

- Importance of Human Error Prevention/reduction

- Training and human error

- Facts about human error

- Human Error as the Root Cause

- What is Human Error?

- How is Human Error controlled?

- Common mistakes: Memory failures, Overconfidence, We believe we are above average, Visual Detection, Vigilance Effectiveness

- Types of error

- Human error rates and measurement

- Trending and tracking

- Prediction

- CAPA effectiveness

Learning Objectives:

- 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

For more information about this conference visit http://www.researchandmarkets.com/research/v9kbvq/how_to_write

Contacts

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Related Topics: Pharmaceutical Manufacturing

Contacts

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900
U.S. Fax: 646-607-1907
Fax (outside U.S.): +353-1-481-1716
Related Topics: Pharmaceutical Manufacturing