#55: Overview of Drug Development

Jun 23 2013 9:00AM - Jun 23 2013 5:00PM | Boston Convention and Exhibition Center 415 Summer Street, Boston, MA 02210 USA

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Learning Objectives

At the conclusion of this tutorial, participants should be able to:

Recognize the process of discovering and developing new pharmaceutical products
Describe the activities associated with conducting clinical research and reporting the results and responsibilities of various departments in accomplishing these activities
Discuss institutional review, informed consent, and financial disclosure
Explain the concepts and functions associated with ensuring overall quality of studies
Describe the organization of the FDA, their authority, and interactions with sponsor companies.

Instructor(s)

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George H. D'Addamio, PhD

President
PharmConsult Inc., United States

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

Participants with Disabilities:
Reasonable accommodations will be made available to persons with disabilities who attend an educational activity. Contact the DIA office in writing at least 15 days prior to event to indicate your needs.

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