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261. Postmarketing adverse event reporting for medical products and dietary supplements during a pandemic

262. Policy for coronavirus disease-2019 tests during the public health emergency (revised): immediately in effect guidance for clinical laboratories, commercial manufacturers, and Food and Drug Administration staff

264. Submission of plans for cigarette packages and cigarette advertisements (revised)

265. Required warnings for cigarette packages and advertisements: small entity compliance guide (revised)

266. Enforcement policy for face masks and respirators during the coronavirus disease (COVID-19) public health emergency (revised): guidance for industry and food and drug administration staff

269. Wholesale distributor verification requirement for saleable returned drug product and dispenser verification requirements when investigating a suspect or illegitimate product: compliance policies

270. Technical considerations for non-clinical assessment of medical devices containing nitinol: guidance for industry and Food and Drug Administration staff