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

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

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

10. Adaptive designs for clinical trials of drugs and biologics

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

12. Administrative rulemaking

13. Administrative rulemaking

14. Adolescent and young adult substance use: federal grants for prevention, treatment, and recovery services and for research : report to Congressional committees

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

17. Allergic rhinitis: developing drug products for treatment

19. Amyotrophic lateral sclerosis: developing drugs for treatment

20. Anthrax: developing drugs for prophylaxis of inhalational anthrax