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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

nlm:nlmuid-101760040-pdf

3. Access to health insurance

nlm:nlmuid-101762170-pdf

5. Adaptive designs for clinical trials of drugs and biologics

nlm:nlmuid-101760568-pdf

6. Administrative rulemaking

nlm:nlmuid-101762303-pdf

7. Amyotrophic lateral sclerosis: developing drugs for treatment

nlm:nlmuid-101760442-pdf

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

nlm:nlmuid-101760477-pdf

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

nlm:nlmuid-101587049-pdf