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Beyond biological evaluation, successful clinical translation of CQDs requires strict adherence to Good Manufacturing Practice (GMP) standards to ensure reproducibility, quality control, and patient safety throughout production [178]

The biggest risks include counterfeit products, contamination, incorrect dosing, poor storage, unknown ingredients, and lack of sterility

It remains to be seen how CMS will handle discussions with states about their existing DSHP and DSIP authority or how states will respond in future Section 1115 waiver proposals and renewals

Manufactured under controlled conditions, it is intended for analytical and laboratory research applications involving peptide-based experimental systems