Technical Writing Best Practices

Duration: 60 Minutes
flat 50% off on this webinar
Technical Writing generally conforms to Good Documentation Practices (GDocP). This term describes standards to create and maintain documents. The term is primarily associated with the pharmaceutical and medical devices industries but applies to documents created in multiple organizations. Most companies have in-house requirements that all documents produced within the organizations conform to the firms' particular requirements. The purpose of this webinar is to define and clarify 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 Best Practices
Instructor: Robert Peoples
Product ID: 505355
Objectives of the Presentation
  • Apply Technical Writing Best Practices to any document
  • Gain insight into Technical Writing Best Practices General Requirements
  • Avoid violations of Technical Writing Best Practices
  • Learn the Technical Writing Best Practices for corrections
  • Learn the Technical Writing Best Practices for the treatment of numbers
  • Learn the Technical Writing Best Practices for the reference of source materials
Why Should you Attend
IT, scientific, human resources and even legal personnel may benefit from learning how to apply the best practices to Technical Writing because the creation of documents applies to all disciplines. Join this webinar to gain valuable insight into how to address this challenge.

Areas Covered
  • Basics of Technical Writing Best Practices
  • Technical Writing Best Practices General Requirements
  • Technical Writing Best Practices for Violations
  • Technical Writing Best Practices for Corrections
  • Technical Writing Best Practices the Treatment of Numbers
  • Technical Writing Best Practices for Reference to Source Materials
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
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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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