Technical Writing for the Pharmaceutical Manufacturing Industry
Duration : 60 Minutes
Carl Patterson, MS, SSGB, SSBB,
Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However Read more
Personnel in Pharmaceutical manufacturing will be asked to review many different documents. These documents are important, in that, they will be scrutinized by regulatory bodies. The aspects of writing these documents are different. The style of writing is more reader-centric, as opposed to writer-centric. Understanding the aspects of reader-centric writing is important in this industry.
Course Objectives:
Writing documents can be a challenge. Join this webinar to gain valuable insight into how to address this challenge. Learn techniques to communicate contributions and ideas developed to stakeholders.
Course Outline:
• The Pharmaceutical manufacturing industry is a very different industry, it is not a study in creative writing. It is an industry that is based on providing fact-based evidence and developing a sound scientific conclusion based on that evidence
• Understanding how to write for the industry is an art, there are few courses that teach how to write for the industry. It is mostly up to the writer to develop a style and technique that is appropriate for the industry
• This course is not an extensive writing course, but an introduction to the documents, various formats, and how to develop the writing component that is needed for the Pharmaceutical Manufacturing industry
• Various example documents will be discussed: Investigations (deviations and other quality system documents), facility reports, environmental monitoring reports, validation reports, validation protocols, etc
• What to look for when reviewing documents
What You Get:
• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points
Who Will Benefit:
• Scientists, engineers, and technicians in research and development
• Quality assurance (QA)
• Information technology (IT)
• Manufacturing
• Quality Control
• Auditors
• Other operations professionals
• Administrative staff that must prepare documentation in support of R&D and operations activities
• Anyone who wants an in-depth and comprehensive overview of the structure of the language and writing within the broad range of reporting that the industry requires
• Validation
Please reach us at 1-888-844-8963 for any further assistance or if you wish to register
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LIVE : Scheduled on
13-January-2025 :01:00 PM EST
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