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FDA Pathways Offer Faster Track for Oncology Drug Development

For biotech companies advancing oncology therapies, regulatory speed can be critical to achieving key milestones and getting new therapies to patients faster. In a recent interview, Josh Taylor, PhD, senior director of regulatory affairs at Allucent, discussed how biotech companies can leverage the FDA’s expedited programs—Fast Track, Breakthrough Therapy, Accelerated Approval and Priority Review—to shorten…

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