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151. Regulatory considerations for human cells, tissues, and cellular and tissue-based products: minimal manipulation and homologous use : guidance for industry and Food and Drug Administration staff

152. Cancer clinical trial eligibility criteria: minimum age considerations for inclusion of pediatric patients : guidance for industry and IRBs

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

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

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

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

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

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