Writing High-Profile Project Evaluation Reports

Philip Vassallo is a Keynote Speaker at Compliance Key, Inc. He has designed, delivered, and supervised communication training programs for more than 20,000 executive, managerial, supervisory, administrative, and technical professionals internationally over the past three decades. Dr. Vassallo has edited major reports for corporations and government, and he has coached numerous writers. He is the author of the books How to Write Fast Under Pressure, The Art of E-Mail Writing, and The Art of On-the-Job Writing. His widely referenced blog Words on the Line offers practical tips for developing wr........


The reality of any professional discipline is this: If it is not in writing, it never happened. All the professional observation and objective review that a clinician puts into an analysis are meaningless unless the work appears in a complete, objective clear, and concise evaluation report. Knowing this truth is obvious; getting there is the challenge.

Why should you attend this webinar?

Writing High-Profile Project Evaluation Reports begins with a practical tool for comprehensively addressing stakeholders concerns about a project or program under review. It continues through issues of organizing content cohesively to ensure a wide range of readers can capture the data that matters to them. Next, the webinar strikes the delicate balance between objectivity and impact by encouraging time-tested best editing practices and discouraging traps that lead to losing credibility. In effect, report writers attending this session will have a means to craft their own high-quality evaluation reports.

Areas Covered in the Session:

Who can Benefit:

This webinar will provide valuable assistance to managers and technical staff who review agencies, programs, or employees, and who write reports, develop action plans, and assess management responses to evaluations in the following disciplines: 
  • Biotechnology
  • Clinical Research
  • Drug Administration
  • Environmental Compliance
  • Laboratory Compliance
  • Regulatory Affairs
  • Safety and Quality

Webinar Id: FSPV003

Training Options:

Duration: 90 mins

 Recorded: [Six month unlimited access]

 $237(Single Attendee)  $599(Unlimited Attendee)

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