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51. Clarification of orphan designation of drugs and biologics for pediatric subpopulations of common diseases

54. Dissolution testing and acceptance criteria for immediate-release solid oral dosage form drug products containing high solubility drug substances

55. Quality attribute considerations for chewable tablets

56. Microdose radiopharmaceutical diagnostic drugs: nonclinical study recommendations

58. Allergic rhinitis: developing drug products for treatment

60. Appropriate use of voluntary consensus standards in premarket submissions for medical devices: guidance for industry and Food and Drug Administration staff