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521. Classification of products as drugs and devices & additional product classification issues: final guidance : guidance for industry and FDA staff

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

523. Compliance policy for required warning statements on small-packaged cigars

524. Center for Devices and Radiological Health appeals processes: questions and answers about 517A : guidance for industry and Food and Drug Administration staff

525. Developing and responding to deficiencies in accordance with the least burdensome provisions: guidance for industry and Food and Drug Administration staff

526. Requests for feedback on medical device submissions: the pre-submission program and meetings with Food and Drug Administration staff : guidance for industry and Food and Drug Administration staff

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

528. Display devices for diagnostic radiology: guidance for industry and Food and Drug Administration staff

529. M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use