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Archived from the original on 4 September 2019

The KYC requirements which can include identity verification beyond what other vendors require create friction that many researchers prefer to avoid

Comment: A few commenters opposed the second alternative policy considered by CMS, which would require manufacturers of Part D rebatable drugs to submit to CMS AMP data for the payment amount benchmark period in cases where the manufacturer did not report AMP under the MDRP for such period, but AMP data are available either for the NDC-9 or for another NDC-9 within the same dosage form and strength

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We proposed to amend 410.152 by adding paragraph (o) to establish the fee schedule and the pricing methodologies used to determine the payment limit for DCAPS drugs under Part B