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21–22 April 2010
Amsterdam, The Netherlands
Speaker: Sunita Prem Ahir, Regulatory Affairs Manager, Devices
Topic: Post Market Clinical Follow-up: Global Requirements
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23–27 April 2010
Tampa, FL
Poster Presenter: Elizabeth Jay, RN, MA
Topic: Pediatric Assent: Key Factors for Forms and Procedures
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23–26 May 2010
Boston, MA
Speaker: Efraim Roe, Executive Director, Medical Devices
Topic: Misconceptions about CROS: You've Heard the Complaints, Now Hear the Reality
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13–17 June 2010
Washington, DC
Booth 1811
Speaker: Charlene Zebrowski, Executive Director, Clinical Trial Management
Topic: Meeting Enrollment Goals in a Competitive Environment: Development, Implementation and Monitoring of Site Patient Recruitment and Enrollment Plans
Speaker: Cindi Stout, Director, CTM Resourcing
Topic: Maximizing Efficiencies in Project Management and Monitoring through a Centralized Resourcing Model
Speaker: Anita Frijhoff, PhD, ELS, Medical Writer
Topic: A Medical Writing Essential: Reviewing Statistical Analysis Plans
Speaker: Marilyn Ingram, Manager Global Medical Writing
Topic: Investigational New Drug (IND) Applications: A Case Study of Document Development from the Medical Writing Perspective
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