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Not for Diagnostic, Clinical, or Therapeutic Applications

Product verification through lab testing reduces contamination risk and supports consistency

Epub 2020 Dec 22

Updates to the Form, Manner, and Timing of ASCQR Program Data Submission In the CY 2026 OPPS/ASC proposed rule, we proposed to establish data submission and reporting requirements for Patient-Reported Outcome-Based Performance Measures (PRO-PMs) for the ASCQR Program, including for the proposed Information Transfer PRO-PM (90 FR 33782)

The diluent for any investigational peptide must always be the one specified in the trial protocol or product dossier