Items 101 ~ 120 of 5552, Page 6 of 279 
  12/20/2018 U.S. FOOD & DRUG ADMINISTRATION - Government
FDA sends warning to company for marketing dangerous unapproved stem cell products that put patients at risk and puts other stem cell firms, providers on notice
- Genetech, Inc. warned about umbilical cord blood-derived cellular products distributed by Liveyon, LLC. FDA is also sending letters to other firms and providers offering stem cell treatments notifying them of agency’s regenerative medicine policy framework.
  12/20/2018 Centers for Disease Control and Prevention - Health and Science
Deadly Marburg Virus Found in Sierra Leone Bats
- First time this Ebola-like virus identified in West Africa
  12/11/2018 Radiological Society of North America - Clinical
Novel Technique May Significantly Reduce Breast Biopsies
- A combination of three-compartment breast image analysis and radiomics may improve cancer diagnosis and reduce breast biopsies...
  11/28/2018 U.S. FOOD & DRUG ADMINISTRATION - Government
FDA approves first biosimilar for treatment of adult patients with non-Hodgkin’s lymphoma
- The agency has now approved 15 biosimilars and is advancing new policies to improve the efficiency of biosimilar development and review
  11/26/2018 U.S. FOOD & DRUG ADMINISTRATION - Health and Science
FDA approves an oncology drug that targets a key genetic driver of cancer, rather than a specific type of tumor
- New drug Vitrakvi targets specific receptor kinase that promotes tumors
  11/26/2018 World Health Organization (WHO) - Public Health
Democratic Republic of the Congo begins first-ever multi-drug Ebola trial
  11/26/2018 U.S. FOOD & DRUG ADMINISTRATION - Government
Statement from FDA Commissioner Scott Gottlieb, M.D. and Jeff Shuren, M.D., Director of the Center for Devices and Radiological Health, on transformative new steps to modernize FDA’s 510(k) program to advance the review of the safety and effectiveness of medical devices
- Modernizing the 510(k) Pathway“Safety and Performance Based Pathway” / Promoting Greater Transparency and Post-Market Surveillance
  11/21/2018 U.S. FOOD & DRUG ADMINISTRATION - Clinical
FDA approves new treatment for patients with acute myeloid leukemia
- The U.S. Food and Drug Administration today approved Daurismo (glasdegib) tablets to be used in combination with low-dose cytarabine (LDAC), a type of chemotherapy, for the treatment of newly-diagnosed acute myeloid leukemia (AML)...
  11/20/2018 Radiological Society of North America (RSNA) - Health and Science
Researchers Use MRI to Predict Alzheimer’s Disease
- MRI assessment of the brain’s white matter using diffusion tensor imaging (DTI) is a promising option for analysis of dementia risk.
  11/19/2018 World Health Organization (WHO) - Public Health
WHO and partners launch new country-led response to put stalled malaria control efforts back on track

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