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271. Evaluation of internal standard responses during chromatographic bioanalysis: questions and answers

272. Drugs for treatment of partial onset seizures: full extrapolation of efficacy from adults to pediatric patients 2 years of age and older

273. Humanitarian device exemption (HDE) program: guidance for industry and Food and Drug Administration staff

275. Citizen petitions and petitions for stay of action subject to section 505(q) of the Federal Food, Drug, and Cosmetic Act

276. Wholesale distributor verification requirement for saleable returned drug product: compliance policy

277. Amyotrophic lateral sclerosis: developing drugs for treatment

278. Changes to existing medical software policies resulting from section 3060 of the 21st Century Cures Act: guidance for industry and Food and Drug Administration staff

279. Bacterial risk control strategies for blood collection establishments and transfusion services to enhance the safety and availability of platelets for transfusion

280. Further testing of donations that are reactive on a licensed donor screening test for antibodies to hepatitis C virus