$299
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Why Should You Attend:
Technical writing in the Pharmaceutical Industry is a highly specialized field. Technical writing differs from general correspondence in that it is written for a specific audience. Technical writing often consists of SOPs and reports but may apply to any documentation written for a restricted group.
Each of us must document our activities to someone within the company. This is particularly true in a highly specialized, highly regulated field like the pharmaceutical industry. Chemists, biologists, engineers, IT personnel Each and statisticians among other highly technical specialists may find writing documents to be a challenge. Join this webinar to gain valuable insight into how to address this challenge. Learn techniques to communicate contributions and ideas developed to stakeholders.
Areas Covered in the Webinar:
- How to begin the process
- How to collect information and determine what information is required
- How to identify and receive contributions from SMEs
- How to write the document
- How to address comments from reviewers
- How to negotiate with reviewers when disagreements arise between reviewers
- How to incorporate comments into the final document
- How to obtain comments in order to address timelines
- Final approval of the document
Who Will Benefit:
- Chemists
- Engineers
- IT personnel
- Any highly technical, highly specialized personnel
Webinar Events
Attend Live Webinar
Aug 20, 2019 - 01:00 PM EDT
Duration: 60 Minutes
Single Attendee
Premier pro price: $269 (save 10%)
Group-Max. 10 Attendees/Location (For Multiple Locations Contact Customer Care) Super Deal - Get CD/USB Drive Free!
Premier pro price: $629 (save 10%)
LIVE + RECORDED VERSION
Premier pro price: $449 (save 10%)
Training CD-DVD
Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment
Premier pro price: $539 (save 10%)
Recorded video
Recorded video session
Premier pro price: $314 (save 10%)
Speaker: Robert Peoples, Retired Technical Writer, Tunnell Consulting Inc
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.
