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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