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Writing and Enforcing Effective SOPs Basics

  October 17, 2018  
CfPA-The Center for Professional Advancement, Online Live
December 13, 2018 at 11:00 a.m.–12:30 p.m. (ET)

Who Should Attend?
This training will benefit professionals in the pharmaceutical, medical device, biotechnology, cosmetic and food industries as well as those in FDA regulated industries. It will be especially valuable to professionals in Quality Assurance, Engineering, Validation and Manufacturing. Directors, Managers, Technical writers and General staff charged with the responsibility for creating, reviewing, approving and implementing written standard operating procedures and instructions will find this course highly beneficial as well.

Course Description
This 90-minute accredited training will address how to write effective Standard Operating Procedures and Work Instructions in support of your company’s activities. You will learn how to organize and deliver information for the intended audience and purpose. You will learn how to write clear and readable documents, and how to revise and refine your own and others’ writing.

Can't Make this LIVE Webinar? 
Simply select the On Demand option when registering and we will send you the link to view the recorded version.

This course will be available On Demand: December 14, 2018
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Joy McElroy, Consultant to the pharmaceutical and biotech industries

With 10 years of experience as a consultant, and over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of Quality Assurance, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualification and Validation Protocols for numerous Companies. Ms. McElroy specializes in Equipment Qualification, Sterilization, Cleaning Validation, and GMP Compliance Auditing. In 2013 Ms. McElroy started her own company, Maynard Consulting Company, which provides top engineers, auditors, and validation specialist to pharmaceutical, biotech and medical device clients worldwide.
Deadline for Abstracts: n/a
Registration: Please click here for registration information.
E-mail: Jmorbit@cfpa.com
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