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Effective and Compliant Technical Writing

 
  October 07, 2019  
     
 
CfPA-The Center for Professional Advancement, Online Live
December 16 2019 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This course is geared toward the industries of Pharmaceutics, Biologics and Medical Device Manufacturing. It is intended for professionals in Analytics, Operations, and Managerial roles. It would be beneficial to those who work in departments such as Quality Assurance, Quality Control, Manufacturing, Engineering and Documentation.

Course Description
This technical writing training program will offer you an understanding of how the reporting process supports products in research, development, and in the marketplace. This 90-minute, accredited training will highlight the mandates for documentation set forth by the regulators, such as the FDA, the ISO, and other governing bodies. The program will train you on effectively reviewing and revising documents and assessing your audience, thus, producing effective written correspondence.

Our LIVE online training offers interactive participation. We highly encourage you to open YOUR microphone during the live course to allow for the free exchange of remarks and questions between attendees and course director.

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.

On Demand available approximately 3 business days after the live offering.
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
   Joy McElroy, Consultant to the pharmaceutical and biotech industries

With 19 years of experience as a consultant, and over 25 years total experience in the pharmaceutical and biotech industries, Joy has gained extensive knowledge of Quality Assurance, Technical Writing, Process and Cleaning Validation, and Equipment Qualification. She has written and executed Equipment Qualifications and Validation Protocols for numerous Companies such as Mallinckrodt, Wyeth Lederle, Merck, BioMerieux, Catalent, and Biotest, Novartis, Imprimis, Cody Laboratories, and Xceilence.

Her knowledge, experience, and strong work ethic have made her a highly sought-after engineer, technical writer, and trainer in both the pharmaceutical and biotech industries. Joy specializes in Equipment Qualification, Cleaning Validation, and GMP Compliance Auditing, and technical writing, and GMP, Audit Preparation, and SOP writing training.

In 2013 Joy started, Maynard Consulting Company, which provided engineers, auditors, and validation specialist to pharmaceutical, biotech and medical device clients across the United States, Canada, and the world.

In 2019 she opened her own company, McElroy Training and Consultancy, LLC which provides consultants for various projects as well as on and off site training to pharmaceutical and biotech companies throughout the United States, Canada, and the world.
 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: Jmorbit@cfpa.com
 
 
   
 
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