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Because research-market material is sold outside any approved supply chain, its identity and purity are unverified: published trial data describe a characterized study drug, not the contents of an arbitrary vial, so identity confirmation (for example by mass spectrometry and HPLC) and a batch certificate of analysis are the minimum a rigorous research setting should require

Quarterly ALL PPS meetings to discuss and clarify currently relevant DSRIP program protocols and progress benchmarks Annual Learning Collaboratives as required by the STCs where PPS can showcase collaborative, transformational and innovative DSRIP activities

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