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Notable interactions include: Many med spa intake processes are streamlined for speed and convenience, which can mean medication review is either rushed or skipped entirely

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In March 2015, FDA approved LIXELLE as a Class III Humanitarian Use Device (HUD) with an approved Humanitarian Device Exemption (HDE)

One commenter suggested that Safety of Care measures may not sufficiently account for clinical complexity, particularly for large tertiary hospitals and those performing high volumes of complex cases, which could obscure meaningful quality differences and discourage hospitals from treating high-risk patients