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13. Severely debilitating or life-threatening hematologic disorders: nonclinical development of pharmaceuticals

14. REMS: FDA's application of statutory factors in determining when a REMS is necessary

15. Oncology pharmaceuticals: reproductive toxicity testing and labeling recommendations

16. Testing of glycerin, propylene glycol, maltitol solution, hydrogenated starch hydrolysate, sorbitol solution, and other high-risk drug components for diethylene glycol and ethylene glycol: guidance for industry