|Articles|December 1, 2008

ONCOLOGY Vol 22 No 14
Volume 22
Issue 14

FDA Approves New Imaging System to Enhance Cervical Cancer Detection

BD Diagnostics recently announced that it received US Food and Drug Administration (FDA) Premarket Approval for the BD FocalPoint GS Imaging System.

BD Diagnostics recently announced that it received US Food and Drug Administration (FDA) Premarket Approval for the BD FocalPoint GS Imaging System. This innovative new system is designed to enhance cervical cancer screening for cytology laboratories using the BD SurePath Pap test slides to detect evidence of squamous carcinoma, adenocarcinoma and their usual precursor conditions.

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The Absent-Minded Professor: An Unusual Complication of Melanoma

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Inflammatory Breast Cancer: A Complex Disease

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Defining the IBC Phenotype

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Acupuncture

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Two Orphan Drug Designations Granted for Reviroc in NHL

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NDA Submitted for Trabectedin to Treat Relapsed Ovarian Cancer

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FDA Considers Update for Tanning Bed Labels

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Fostamatinib Is Well-Tolerated and Has Significant Clinical Activity in Diffuse Large B-Cell Lymphoma and Chronic Lymphocytic Leukemia

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Dexamethasone in Induction Can Eliminate One-Third of All Relapses in Childhood Acute Lymphoblastic Leukemia

almost 17 years ago

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Novel Antifolate Pralatrexate Shows Promise in Patients With Relapsed or Refractory Peripheral T-Cell Lymphoma

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FDA Approves New Imaging System to Enhance Cervical Cancer Detection

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