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2. Consumer perspectives on health care decision-making: quality, cost and access to information

4. The ABCs of APCDs: how states are using claims data to understand and improve care

6. Unique device identification: Policy regarding compliance dates for class I and unclassified devices, direct marking, and Global Unique Device Identification Database requirements for certain devices : guidance for industry and Food and Drug Administration staff

7. Civil money penalties relating to the ClinicalTrials.gov data bank: guidance for responsible parties, submitters of certain applications and submissions to FDA, and FDA staff