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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

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

5. Adaptive designs for clinical trials of drugs and biologics

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

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

9. Allergic rhinitis: developing drug products for treatment

10. Amyotrophic lateral sclerosis: developing drugs for treatment