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How can the Promoting Interoperability performance category balance robust Public Health and Clinical Data Exchange objective requirements with our desire to reduce burden on MIPS eligible clinicians

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Therefore, we are continuing our currently approved per response time estimates for submitting the MVP quality performance category data due to this proposal

CMS continues to be interested in comments on this topic and welcomes additional comments on this approach and alternative approachesspecifically, how CMS should address the situations in which the manufacturer of a Part D rebatable drug does not have an MDRP agreement in effect for any part of the applicable period or when a Part D rebatable drug may be excluded from the definition of a COD and manufacturers may not be required to report pricing and drug product information under section 1927(b)(3) of the Act