Technical Writer Training

Duration: 60 Minutes
flat 50% off on this webinar
Technical writing in is a highly specialized field. Hands-on training is absolutely necessary in this field. Yet there are strategies that can be applied such that this training is not overwhelming. Training for technical writing includes the use of global English, ignoring word count and the use of graphics. The purpose of this webinar is to train technical writers in general guidelines for the creation and maintenance of documents in order to ensure consistency between documents created by various functional groups within organizations.
Technical Writing
Instructor: Robert Peoples
Product ID: 509352
Objectives of the Presentation
  • Creating technical documents
  • Define and address the target audience
  • Comparison of technical writing and creative writing and/or journalism
  • Parts of a technical document
  • Editing/proofreading techniques
  • Technical writing concerns
Why Should you Attend
IT, scientific, human resources and even legal personnel may benefit from training in the principles and practices of technical writing because the creation of documents applies to all disciplines. Join this webinar to gain valuable insight into how to address these challenges.

Areas Covered
  • Learn about technical document issues
  • Learn technical writing goals
  • Learn how to research the subject matter and audience
  • Learn how technical writing differs from creative writing
  • Learn how to edit/proofread technical writing (rewriting)
  • Learn the value of charts, graphs, pictures and tables
  • Learn to create in-house templates
  • Things to avoid in technical writing
  • Roles of reviewers and approvers
Who will Benefit
  • IT Personnel
  • Scientific Personnel
  • Human Resources
  • Any highly specialized company personnel
  • Chemists
  • Engineers
  • Any highly technical, highly specialized personnel
  • Scientists, engineers, and technicians in research and development
  • Quality assurance (QA)
  • Information technology (IT)
  • Manufacturing
  • 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
$375
Recorded Session for one participant
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  $500.00 Training CD
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  $600.00 Training USB Flash Drive
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How it works
Live Session - How it works
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  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
After obtaining a B.S. and an M.S. in Chemistry from Tuskegee University, Robert Peoples joined the pharmaceutical industry as a Research Chemist with a concentration in analytical chemistry at Wyeth/Lederle. While at Wyeth/Lederle Robert was primarily responsible for the analysis of the Active Pharmaceutical Ingredient (API) in various drug delivery formulations, e.g. aerosols, capsules, creams, ointments and tablets. He joined Organon/Merck as a Research Chemist responsible for the development of stability-indicating methods of analysis using HPLC.

While at Organon/Merck, Robert transitioned into technical writing. As a Technical Writer he was responsible for the creation of procedures for instrument qualification, test scripts, IQ/OQ/PQ protocols for sample handling, cleaning validation reports, method transfer reports, method validation reports, stability reports, Change Control and CAPAs. Later he joined Johnson and Johnson as a Technical Writer where he created stability strategies, protocols and reports as well as SOPs, developed training materials and competency profiles in addition to proofreading and improving written reports for other departments. He also edited policies and procedures, user guides, and job aids.

After leaving Johnson and Johnson Robert became a consultant to other pharmaceutical companies where he created SOPs for analytical method validation as well as pharmaceutical stability studies and stability program management. For another client company he created stability reports that addressed FDA concerns about OOS/OOT results. For yet another client company he created stability reports, protocols and strategies for medical devices. He also created written assessments for software-controlled laboratory instrumentation.

Robert also has extensive experience in data review, stability management and training.
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