home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
  HUM-MOLGEN -> Events -> Meetings and Conferences  

Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs) - Webinar By GlobalCompliancePanel

  April 06, 2011  

GlobalCompliancePanel, Online Training Webinar

Overview: This webinar is designed to outline the characteristic of an effective work instruction, and Standard operating procedure.

The webinar is also designed to help differentiate Work Instructions from Standard operating procedures. Attendees will learn the steps used to write effective work instructions and Standard operating procedures.

Why Should You Attend: The current shift in FDA thinking is that manufactures do not give their employees enough direction to perform their jobs. This thinking is reflected in many warning letters that written to organizations by several FDA field offices. The problem is compounded by the confusion in the pharmaceutical, Biotech, and Medical device organizations as to what a Standard operating procedure is, and what a Work Instruction is.

Areas Covered In the Session:
  • How to write a work instruction
  • How to write a standard operating procedure
  • Properties of an effective work instruction
  • Properties of an effective Standard operating procedure
  • The differences between work instructions and Standard operating procedures.
Who will benefit:
  • Quality managers
  • Quality Engineers
  • Process Engineers
  • Manufacturing Engineers
Organized by: GlobalCompliancePanel
Invited Speakers: Mr. Muchemu has over fifteen years experience in Medical Device, Pharmaceutical, Biomedical and Tissue industries as CAPA Training Instructor, Process validation Instructor, Change control Instructor, and CGMP consultant. He has held major positions at Abbott labs, Genentech, Boston Scientific, and Johnson and Johnson. He holds degrees in Biology, Chemical Engineering, and is currently working an MBA with a concentration in Public Health. He is an established author of several GMP books.
Deadline for Abstracts: 2011-05-05
Registration: Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00
E-mail: webinars@GlobalCompliancePanel.com
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.