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Technical Writing: A Detailed Process

Tuesday, 12 November 2019 10:00 AM PST | 01:00 PM EST

Training Duration = 60 min               Sponsored by ComplianceOnline

Click Here to register $229.00

Click Here to register and receive CD recording $399.00

Technical Writing: A Detailed Process provides step-by-step instructions for experienced Technical Writers go from the blank screens to the final written presentations.

The webinar includes procedures for the creation of document plans and meetings with stakeholders to produce the highest quality of Technical Documents. It provides guidance on the conversion of highly technical material into language easily understood by the general public.

Why Should You Attend:

Experienced Technical Writers who specialize in science, engineering, Information Technology and statistics among other highly technical specialties will find in this webinar organizational tips and suggestions that benefit them with their daily responsibilities.

These professionals will find guidance to better organize their time and expertise to create higher quality documents within increasingly tight timeliness. Without the suggestions provided in the webinar precious time can best lost in creating high quality documents.

Because of increasingly short timelines none of us has enough time to create the best documents that utilize our best efforts. Join this webinar to learn step-by-step instructions on how to create better documents in less time as well as learn techniques to communicate contributions and ideas developed to stakeholders, reviewers and approvers.

Areas Covered in the Webinar:

  • How to plan the document process from initiation to final approval
  • How to create the document using an outline or table of contents
  • How to write the first draft and revisions as necessary
  • How to conduct author’s initial review before the formal review process
  • How to respond to reviewers and approvers
  • How to accept positive and negative comments from reviewers/approvers
  • How to negotiate when disagreements arise between reviewers/approvers
  • How to incorporate comments into the final document
  • How to obtain comments in accordance with required timelines
  • Final approval of the document

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.