How to write error free procedures and comply with GMP regulations

Website https://www.demystifiedsolutions.com/trainingDetails/How-to-write-error-free-procedures-and-comply-w | Edit Freely

Category

Deadline: July 18, 2017 | Date: July 18, 2017

Venue/Country: Online

Updated: 2017-03-10 17:29:59 (GMT+9)

Call For Papers - CFP

Areas Covered in this Webinar

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

Learning Objectives

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.

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

For More Info, Please Click below URL:

https://www.demystifiedsolutions.com/trainingDetails/How-to-write-error-free-procedures-and-comply-with-GMP-regulations-DEMY050130