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152. Cancer clinical trial eligibility criteria: patients with organ dysfunction or prior or concurrent malignancies

153. Marketing status notifications under Section 506I of the Federal Food, Drug, and Cosmetic Act: content and format

154. Enforcement priorities for electronic nicotine delivery systems (ENDS) and other deemed products on the market without premarket authorization (revised)

155. Temporary policy regarding accredited third-party certification program onsite observation and certificate duration requirements during the COVID-19 public health emergency

156. Temporary policy on repackaging or combining propofol drug products during the COVID-19 public health emergency

157. Recommendations to reduce the possible risk of transmission of Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob disease by blood and blood components

160. Temporary policy for compounding of certain drugs for hospitalized patients by pharmacy compounders not registered as outsourcing facilities during the COVID-19 public health emergency (revised)