Technical writing usually follows Good Documentation Practices (GDocP), the standards for creating and maintaining documents. The term is linked most closely with pharmaceutical and medical device companies, but the same principles apply in many organizations.
This 60-minute technical writing best practices training defines general guidelines for creating and maintaining documents so that work from different functional groups stays consistent, alongside your company's own in-house requirements.
You'll cover the basics and general requirements, how to avoid violations, how to make corrections, how to treat numbers, and how to reference source materials.
Every discipline produces documents, so IT, scientific, HR and even legal staff can benefit from applying consistent technical writing practices.
This session suits chemists, engineers, scientists and technicians in R&D, QA, IT, manufacturing and operations professionals, HR, and administrative staff who prepare documents supporting R&D and operations.
Every discipline produces documents, so IT, scientific, HR and even legal staff can benefit from applying consistent technical writing practices.
This session suits chemists, engineers, scientists and technicians in R&D, QA, IT, manufacturing and operations professionals, HR, and administrative staff who prepare documents supporting R&D and operations.
Robert Peoples
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, …
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