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1. 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


3. Access to health insurance


5. Adaptive designs for clinical trials of drugs and biologics


6. Administrative rulemaking


7. Amyotrophic lateral sclerosis: developing drugs for treatment


8. Bacterial risk control strategies for blood collection establishments and transfusion services to enhance the safety and availability of platelets for transfusion


10. Bending the obesity cost curve: reducing obesity rates by five percent could lead to more than $29 billion in health care savings in five years