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9 Mar 2016, 7:58 am by Daily Record Staff
He is leading a team of board-certified radiologists and technicians who provide patient-centered, innovative diagnostic services in three separate divisions: diagnostic radiology, nuclear medicine and interventional radiology. [read post]
11 Jan 2009, 7:45 pm
CNN is reporting that nine scientists at the Food and Drug Administration's Center for Devices and Radiological Health (CDRH) have written a six-page letter to President-elect Barack Obama and his transition team, alleging gross mismanagement at the agency that has "placed the American public at risk. [read post]
8 Apr 2011, 2:37 am by Tom D'Amore
In a recent article in Radiology, David Brenner, PhD, DSc, of the Center for Radiological Research at Columbia University Medical Center, in New York, and David Schauer, ScD, CHP, executive director of the National Council on Radiation Protection and Measurements, offered their views on the subject of the radiation risk posed by airport scanners. [read post]
13 Nov 2006, 11:12 am
The Center for Devices and Radiological Health within the federal Food and Drug Administration is taking steps to increase its ability to identify, analyze, and act on postmarket information in order to improve the safety and effectiveness of medical devices... [read post]
18 Nov 2008, 11:52 am
Ed Silverman reports that the House Energy and Commerce Committee is investigating allegations that managers at the FDA Center for Devices and Radiological Health have "corrupted and interfered with the scientific review of medical devices. [read post]
3 Aug 2011, 12:26 pm
  The study was co-authored by Yulin Ge, M.D., Associate Professor in the Department of Radiology at NYU Langone Medical Center. [read post]
18 Jan 2007, 7:17 am
" The Illinois attorney general's office claims that more than 20 Chicago-area radiology centers engaged in a widespread scheme to win... [read post]
18 Feb 2016, 3:50 pm by Jay W. Belle Isle
Jeffrey Shuren, Director, Center for Devices and Radiological Health for the FDA in which a congressman questions FDA over Essure Data.The post Congressman Questions FDA Over Essure Data and Alleged Kickbacks appeared first on Legal Reader. [read post]
8 Feb 2024, 10:00 pm
The US Food and Drug Administration’s (FDA’s) Center for Devices and Radiological Health recently announced its intention to reclassify certain high-risk in vitro diagnostic devices (IVDs) as moderate risk, a potential first step as the agency prepares to oversee laboratory-developed tests (LDTs). [read post]
8 Feb 2024, 10:00 pm
The US Food and Drug Administration’s (FDA’s) Center for Devices and Radiological Health recently announced its intention to reclassify certain high-risk in vitro diagnostic devices (IVDs) as moderate risk, a potential first step as the agency prepares to oversee laboratory-developed tests (LDTs). [read post]
8 Feb 2024, 10:00 pm
The US Food and Drug Administration’s (FDA’s) Center for Devices and Radiological Health recently announced its intention to reclassify certain high-risk in vitro diagnostic devices (IVDs) as moderate risk, a potential first step as the agency prepares to oversee laboratory-developed tests (LDTs). [read post]
8 Feb 2024, 10:00 pm
The US Food and Drug Administration’s (FDA’s) Center for Devices and Radiological Health recently announced its intention to reclassify certain high-risk in vitro diagnostic devices (IVDs) as moderate risk, a potential first step as the agency prepares to oversee laboratory-developed tests (LDTs). [read post]
8 Feb 2024, 10:00 pm
The US Food and Drug Administration’s (FDA’s) Center for Devices and Radiological Health recently announced its intention to reclassify certain high-risk in vitro diagnostic devices (IVDs) as moderate risk, a potential first step as the agency prepares to oversee laboratory-developed tests (LDTs). [read post]
8 Feb 2024, 10:00 pm
The US Food and Drug Administration’s (FDA’s) Center for Devices and Radiological Health recently announced its intention to reclassify certain high-risk in vitro diagnostic devices (IVDs) as moderate risk, a potential first step as the agency prepares to oversee laboratory-developed tests (LDTs). [read post]
25 Apr 2014, 12:59 pm by Debra A. McCurdy
Riley Earlier this week, FDA’s Center for Devices and Radiological Health (CDRH) published two separate draft guidance documents to advance the dual goals of FDA and industry to provide pathways for medical devices to reach the market quickly while ensuring the safety and efficacy of the product. [read post]
1 Feb 2010, 2:22 am by Cal Warriner
The FDA recently announced plans to hold a public meeting entitled “Strengthening the Center for Devices and Radiological Health’s 510(k) Review Process. [read post]
10 Jul 2017, 2:45 pm by Sean Wallace
., has joined of The Tyanna O’Brien Center for Women’s Imaging at Mercy Medical Center. [read post]