CfPA - The Center for Professional Advancement, New Brunswick, NJ
February 1-3, 2010
Who Should Attend
This course is intended for professionals in the pharmaceutical and allied industries who must write or revise documents that are integral to product development and production. It is ideal for those in
• Research & Development
• Quality Control
• Regulatory/Compliance
• Validation
This includes, but is not limited to
• Engineers
• Scientists
• Chemists
• Technicians
This course is also intended for those who wish to gain better writing skills and learn more effective ways to deliver technical information. Description
This practical course will teach you the basic steps in preparing those written documents most frequently required in the pharmaceutical and related industries. Through lectures, discussions and workshops, you will learn to work your way through the writing process to express complex ideas clearly and to organize your writing into standard forms such as memos, letters, proposals and reports. You will also learn strategies for revising, editing and documenting your work.
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