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Titles
- Clinical investigations for prostate tissue ablation devices: guidance for industry and Food and Drug Administration staff1
- Feasibility and early feasibility clinical studies for certain medical devices intended to therapeutically improve glycemic control in patients with Type 2 Diabetes Mellitus: guidance for industry and Food and Drug Administration staff1
- General clinical pharmacology considerations for neonatal studies for drugs and biological products1
- Human gene therapy for neurodegenerative diseases: guidance for industry1
- Patient engagement in the design and conduct of medical device clinical studies: guidance for industry, Food and Drug Administration staff, and other stakeholders1
- Pediatric study plans: content of and process for submitting initial pediatric study plans and amended initial pediatric study plans1
- Procedures for handling post-approval studies imposed by premarket approval application order: guidance for industry and Food and Drug Administration staff1
- The materia medica in its scientific relations1
- The mortality of acute lobar pneumonia: from a study of all the cases of this disease treated at the Massachusetts General Hospital from the first case, in 1822, up to the present day1