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Symposium on Open Source Drug Discovery

23 August 2010, Boston, MA, United States


Introduction
Open-source Drug Discovery is an adaptation to drug R&D of the very successful open-source software model. It has inspired the redesign of the aging pharmaceutical R&D model, and has been used to energize drug research into neglected and rare diseases. Its major features and benefits are:
Enhanced innovation through broader cross-pollination; Much lower costs from leveraging networks of volunteers; Greater speed from faster decision-making; Extremely light and efficient organization. In the last year, the open-source drug R&D model has delivered its first approved drugs (for malaria), and built-up a significant pipeline (for many rare and neglected diseases). There will be speakers from institutions including CSIR (India), WHO, NIH and GlaxoSmithKline.
Venue
240th National American Chemical Society Meeting

240th National American Chemical Society Meeting, Boston, MA, United States

Organised by
Richard W. Harper, Ph.D., MRSC and Bernard Munos
Contact information
Dr Richard Harper
Indiana University-Purdue University Indianapolis, Department of ¾ÅÖÝÓ°Ôº and Chemical Biology, 402 Blackford St LD326, Indianapolis, IN, 46202, United States of America
(317) 418-6924
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