
In today's ACT Brief, we examine FDA input sought on early-phase ibogaine protocols, why mixed outsourcing models spread faster than oversight infrastructure, and a major partnership for a rare kidney disease treatment.
CTTI is announcing it has been engaged by the FDA to support its Patient Engagement Collaborative. This collaborative aims at discussing ways in which patients can participate in the FDA's regulatory discussions about medical products. With patient feedback, this collaborative was created and will continue to be used in the future by bringing together representatives to discuss topics on how patients and the FDA can continue working with one another.
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