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
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
Speakers
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.
