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:
Recently Asked Questions & Answers:
Before starting the first or rough draft, ask yourself the following questions:
Use all the information you gathered and write down all these ideas, concepts and concerns without worrying about the style, grammar, punctuation, organization or anything else. Then proofread, correct, change, add or subtract them from the first draft until it answers the above questions.
Pictures that address the questions listed above should be included in the first draft.
You should first validate the concerns of the reviewers and show the information from the document or source information that supports the document’s point of view.
It is your responsibility to negotiate, to cajole, to coax or do whatever is necessary to obtain consensus between reviewers including soliciting input from upper management.
Who Will Benefit:
From Pharmaceutical, Engineering, IT and highly specialized, highly technical industriesInstructor 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.
This webinar will define the complete technical document creation process. It includes all steps to be made by experienced Technical Writers to create the highest quality Technical Documents. It includes the creation of document plans and organizational meetings with stakeholders and reviewers. Since Technical Writing is a complicated process that is as much art as science the webinar assists Technical Writers to accomplish their daily tasks. It recognizes that Technical Writing is a balancing act between being precise enough to cover the subject matter yet general enough to apply to other locations and/or projects. It also reminds experienced attendees that Technical Writing always includes reviewers and approvers of different levels of expertise in the subject matter. Join the webinar to gain in-depth guidance to create the highest quality documents.
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