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Research vendors describe themselves as chemical suppliers rather than compounding pharmacies under FDA sections 503A and 503B

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This involves comprehensive preclinical testing, multiple phases of human clinical trials, and stringent manufacturing quality control

This initiative follows a rise in U.K

Although we are not finalizing adoption of the Information Transfer PRO-PM, we appreciate the commenters' recommendations and will consider available language options for the Information Transfer PRO-PM if we decide to propose this measure in the future

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