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Start Over You searched for: Subjects United States. Department of Health and Human Services. Remove constraint Subjects: United States. Department of Health and Human Services. Copyright Public domain Remove constraint Copyright: Public domain Publication Year 2000 to 2024 Remove constraint Publication Year: <span class="from" data-blrl-begin="2000">2000</span> to <span class="to" data-blrl-end="2024">2024</span>

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382. Oncology therapeutic radiopharmaceuticals: nonclinical studies and labeling recommendations

384. Osteoporosis: nonclinical evaluation of drugs intended for treatment

385. Placebos and blinding in randomized controlled cancer clinical trials for drug and biological products

386. Factors to consider when making benefit-risk determinations in medical device premarket approval and de novo classifications: guidance for industry and Food and Drug Administration staff

387. Consideration of uncertainty in making benefit-risk determinations in medical device premarket approvals, de novo classifications, and humanitarian device exemptions: guidance for industry and Food and Drug Administration staff

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

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

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