Technical Writing for the Pharmaceutical Manufacturing Industry

01:30 PM ET | 10:30 AM PT | 12:30 PM CT Duration 60 Minutes

Webinar Includes : All the training handouts , certificate ,Q/A and 60 mins Live Webinar

"Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance Professional who is based in San Diego, California"

Writing is more reader centric, as opposed to writer centric

Description

Personnel in the Pharmaceutical manufacturing will be asked to write and review many different documents. These documents are important, in that, it will be scrutinized by regulatory bodies and will paint a picture of the compliance level within a company. The perspective of writing these documents are different from the traditional writing methods. This style of writing is more reader centric, as opposed to writer centric. By understanding why, the aspects of reader centric writing is important in this industry, the participant will be able to present a picture on the compliance level of the company.

Areas Covered

•      Provide information on the various documents within the Pharmaceutical Manufacturing Industry
•      Discuss the format of various documents within the Pharmaceutical Manufacturing industry
•      Discuss the concepts the writer must keep in mind when writing a technical document
•      Discuss any regulatory requirements and what regulatory bodies are looking for when reviewing                                  technical documents Why the review process is important
•      Provide examples of documents reviewed by regulatory bodies and discuss key points of those documents.

Who will Benefit

•      Quality Assurance
•      Validation
•      Quality Control Auditors
•      Manufacturing Personnel
•      Quality Control Personnel

Industries who can attend

This 60 minute online course is intended for professionals in the Pharmaceutical and Biopharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.


Speaker Profile

Carl Patterson, M.S.

Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance Professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However, his avid interest in all things biology, microbiology, and biochemistry officially began when he served in the U.S. Army as a Preventative Medicine Specialist and a Licensed Vocational Nurse. Furthermore, Carl holds various degrees and certifications, including an M.S. in Biomedical Quality Systems from San Diego State University, a B.S. in Microbiology from the University of Texas, and Specialized Certificates in QA/QC & Biotechnology from UCSD.

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