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371. Appeal options available to mammography facilities concerning adverse accreditation decisions, suspension/revocation of certificates, or patient and physician notification orders: guidance for mammography facilities and Food and Drug Administration staff

376. Expansion cohorts: use in first-in-human clinical trials to expedite development of oncology drugs and biologics

377. Center for Devices and Radiological Health (CDRH) appeals processes: Guidance for industry and Food and Drug Administration staff

379. Current good manufacturing practice and preventive controls, foreign supplier verification programs, intentional adulteration, and produce safety regulations: enforcement policy regarding certain provisions

380. Initiation of voluntary recalls under 21 CFR Part 7, subpart C: guidance for industry and FDA staff