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21 May 2025 - 06:30 am

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Vlagom

21 May 2025 - 05:36 am

Hi
Is the FDA's IND process becoming obsolete in the age of digital innovation? As pharmaceutical companies increasingly adopt advanced technologies and automation, could the traditional submission process be replaced or significantly streamlined? What implications might this have for patient access to new therapies?

Vlagom

21 May 2025 - 02:10 am

hi
Is the FDA IND application process a necessary hurdle for innovation, or does it stifle potential breakthroughs in medicine? Consider the implications of rigorous regulations on the speed of drug development and patient access to new therapies. What balance should be struck between safety and innovation?

Vlagom

20 May 2025 - 09:28 pm

Hi
What if the FDA were to introduce a completely automated approval process for IND submissions? Would this enhance efficiency, or could it lead to unforeseen risks in drug safety?

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