With increasingly rapid timelines for achieving IND-ready processes, a bottleneck has emerged in the provision of toxicology data to support INDs for new therapeutics and hence delivery of FIH studies, as Alejandro Fernandez Martell and James Berrie explain in this Drug Target Review article.
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Author(s):
James Berrie
Technical Director, Global Process Development
Alejandro Fernandez-Martell
Principal Scientist, Global Process Development
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