| |
|
|
| |
|
|
| |
HUM-MOLGEN
-> Events
-> Courses and Workshops |
|
|
| |
| |
| |
May 17, 2019 |
|
|
| |
|
|
| |
|
|
|
CfPA-The Center for Professional Advancement, Edison, NJ or Virtually
October 21-22, 2019
Who Should Attend?
This course will benefit professionals from new hires to managers in the pharmaceutical, medical device, biologics and related health industries
who would like to write more effective documents. It is a valuable course for
those in:
• Clinical Research
• Product Development
• Regulatory
• QA/QC
• Compliance
• Manufacturing
• Engineers/Scientists
• Directors and Managers
• New Hires Course Description
|
|
|
|
|
|
|
|
Organized by:
|
|
CfPA-The Center for Professional Advancement |
|
|
Invited Speakers:
|
|
 Zeinab Schwen, President, Strategic Regulatory Consulting |
Zeinab Schwen has over 38 years of experience in the pharmaceutical and medical device industries. After working for major pharmaceutical companies, she founded a successful consulting and medical communications company which has been supporting the health care industry for over 27 years. In her capacity as the President of Strategic Regulatory Consulting she has provided product development, regulatory consulting, submission assistance, and medical communications services to companies nationwide. Ms. Schwen has also taught at several Universities and has led numerous regional workshops on medical, technical, and regulatory writing.
|
|
|
|
|
|
|
|
Deadline for Abstracts:
|
|
n/a
|
|
|
|
|
|
|
|
Registration:
|
|
Please click here for registration information.
|
|
|
E-mail:
|
|
Jmorbit@cfpa.com
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
|
|
|
|
|
|
|
|
|
|
|
|
Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp,
Frank S.
Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved.
Liability, Copyright and Imprint. |
|
This practical two-day accredited course will teach you methods to evaluate your writing style and apply steps to express complex ideas more clearly and concisely. Through lectures and class exercises you will learn strategies for organizing, revising, editing, and proofing documents and correspondences. Essential elements of technical report sections will also be discussed as well as how to respond to FDA requests for information.