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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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May 29, 2012 |
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Pennsylvania Convention Center, Philadelphia, PA USA
Jun 24 2012 9:00AM - 5:00PM
This course takes a practical approach to creating clinical study reports, from data collection to final approval. Learn how to prepare a Clinical Overview for pharmaceutical products (drugs and biologics). In accordance with International Conference on Harmonisation (ICH) guidelines, this in-depth course provides all the information on how to develop Module 2.5 of a Common Technical Document (CTD). EVENT CODE:12402
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Organized by:
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DIA |
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Invited Speakers:
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Patricia A. Matone, PhD President
Scientific Information Services LLC, United State
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Deadline for Abstracts:
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N/A
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Registration:
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Registration Vicki Adkinson Phone: +1-215-442-6162 Email: Vicki.Adkinson@diahome.org Agenda and Event Details Colleen Buckley Phone: +1-215-442-6108 Email: Colleen.Buckley@diahome.org
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E-mail:
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Colleen.Buckley@diahome.org
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