Guestbook

Vlagom

20 May 2025 - 06:15 pm

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Is the FDA IND submission process stifling innovation in the biotech industry? How can we expedite drug development without compromising safety, and is it time to rethink the regulations that govern this essential pathway?

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20 May 2025 - 01:17 pm

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Vlagom

20 May 2025 - 12:59 pm

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Frankhaw

20 May 2025 - 10:52 am

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Is the FDA's IND application process becoming obsolete in the age of decentralized clinical trials? With advancements in technology and the rise of alternative regulatory pathways, should we reconsider the necessity of traditional IND submissions? What implications would this have for innovation in drug development?

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Vlagom

20 May 2025 - 09:28 am

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In a world where pharmaceutical innovations are rapidly evolving, how can the FDA IND process adapt to ensure that groundbreaking treatments reach patients without unnecessary delays? Are there ways to streamline approvals while maintaining safety and efficacy standards?