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Elihu H. Estey, MD, professor of medicine, University of Washington School of Medicine, Fred Hutchinson Cancer Research Center, discusses a potential change to the FDA approval process as it relates to Mylotarg (gemtuzumab ozogamicin).

In a recent blog post and echoed on the Centers for Medicare & Medicaid Services (CMS) web site, Robert Tagalicod, director of the CMS Office of E-Health Standards and Services and acting National Coordinator for Health Information Technology Jacob Reider, MD, announced that the deadline for stage 2 of the meaningful use program would be extended through 2016.