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Quot;INDquot; refers to the preparation of an IND application, the process by which a drug is submitted to the FDA to receive approval for human testing. quot;Phase Iquot; refers to the stage in which compounds are tested for safety, maximal tolerated dose and pharmacokinetics in volunteers without the disease. quot;Phase IIquot; refers to the initial stages of compound testing in patients with the disease or symptoms of interest for ultimate New Drug application (quot;NDAquot;) approval and labeling. This stage first demonstrates the compound's efficacy and dosing range and expands the safety profile. quot;Phase IIIquot; refers to the rigorously controlled test of a new drug in a large population of patients with the disease.

Now, the Mammography Quality Standards Act has expired. But as Congress moves to renew a statute that has helped make early breast cancer detection far more widespread, lawmakers have taken on a tougher task than the first time around.]