fda warning bpc-157 unapproved new drug Peptide Compounding Vote Raises Questions for Developers FDA panel narrowly backs unapproved

Data Submission and Reporting Requirements for the Information Transfer PRO-PM In the CY 2026 OPPS/ASC proposed rule, we discussed the proposed adoption of the Information Transfer PRO-PM beginning with voluntary reporting for the CY 2027 and CY 2028 reporting periods followed by mandatory reporting beginning with the CY 2029 reporting period/CY 2031 payment determination (90 FR 33776 through 33779)

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