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4. 30-Day notices, 135-day premarket approval (PMA) supplements and 75-day humanitarian device exemption (HDE) supplements for manufacturing method or process changes: guidance for industry and Food and Drug Administration staff

7. ACF cannot ensure that all child victims of abuse and neglect have court representation

8. ACOs' strategies for transitioning to value-based care: lessons from the Medicare shared savings program

12. Accelerating adoption of assistive technology to reduce physical strain among family caregivers of the chronically disabled elderly living at home

14. Access and use of electronic health information by individuals with cancer: 2017-2018

16. The Accreditation Scheme for Conformity Assessment (ASCA) Pilot Program: guidance for industry, accreditation bodies, testing laboratories, and Food and Drug Administration staff

17. Acne vulgaris: establishing effectiveness of drugs intended for treatment

18. Adaptive designs for clinical trials of drugs and biologics

19. Addressing teen pregnancy risks for youth living in out-of-home care: implementing POWER through choices 2010 : implementation report

20. Administrative procedures for CLIA categorization: guidance for industry and Food and Drug Administration staff