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

43. Quality attribute considerations for chewable tablets

44. Microdose radiopharmaceutical diagnostic drugs: nonclinical study recommendations

46. Allergic rhinitis: developing drug products for treatment

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

49. Unique device identification: policy regarding compliance dates for class I and unclassified devices : immediately in effect guidance for industry and Food and Drug Administration staff