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301. Live case presentations during investigational device exemption (IDE) clinical trials: guidance for institutional review boards, industry, clinical investigators, and Food and Drug administration staff

302. Metal expandable biliary stents: premarket notification (510(k)) submissions : guidance for industry and Food and Drug Administration Staff

306. Oncology therapeutic radiopharmaceuticals: nonclinical studies and labeling recommendations

308. Osteoporosis: nonclinical evaluation of drugs intended for treatment

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

310. 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