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3. 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

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

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

8. Adaptive designs for clinical trials of drugs and biologics

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

10. Advancement of emerging technology applications for pharmaceutical innovation and modernization

11. Adverse events in long-term-care hospitals: national incidence among Medicare beneficiaries

12. Affordable Care Act: IRS should mitigate limitations of data to be used for the age and gender adjustment for the tax on high-cost health plans : report to Congressional committees

13. The aging services network: accomplishments and challenges in serving a growing elderly population

14. Air ambulance: data collection and transparency needed to enhance DOT oversight : report to the Committee on Transportation and Infrastructure, House of Representatives

16. Allergic rhinitis: developing drug products for treatment

17. Amyotrophic lateral sclerosis: developing drugs for treatment

18. An analysis of private-sector prices for hospital admissions

20. Anthrax: developing drugs for prophylaxis of inhalational anthrax