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Regulatory: Page 82
FDA clears mobile version of Voyant's TraumaCad
By
AuntMinnie.com staff writers
Voyant Health has received U.S. Food and Drug Administration clearance for its TraumaCad Mobile digital templating software for mobile devices.
March 26, 2015
House passes SGR repeal bill
By
AuntMinnie.com staff writers
In a vote of 392 to 37, the U.S. House of Representatives today passed a bill that would repeal the sustainable growth rate (SGR) formula. Of the total yes votes, 212 were from Republicans and 180 were from Democrats.
March 25, 2015
Canada clears IMRIS' Visius iCT
By
AuntMinnie.com staff writers
Image-guided therapy developer IMRIS has received Canadian clearance to market its Visius iCT system.
March 25, 2015
FDA sends MRI recall notices to GE, Siemens
By
AuntMinnie.com staff writers
The U.S. Food and Drug Administration has sent recall letters to GE Healthcare and Siemens Healthcare regarding the operation of some MRI scanners.
March 25, 2015
ACNM endorses end of CED for NaF-PET
By
AuntMinnie.com staff writers
The American College of Nuclear Medicine (ACNM) has thrown its support behind a proposal for national coverage of sodium fluoride (NaF) PET imaging in the U.S. and an end to the coverage with evidence development (CED) requirement for reimbursement.
March 24, 2015
Florida Hospital pays $5.4M to settle federal lawsuit
By
AuntMinnie.com staff writers
The company that operates the Florida Hospital health system has agreed to pay $5.4 million to settle charges filed by the U.S. government that it violated federal rules requiring supervision of radiation oncology services.
March 19, 2015
HHS publishes proposed rule for stage 3 MU
By
Brian Casey
The U.S. Department of Health and Human Services (HHS) Office of the National Coordinator for Health Information Technology has published a proposed rule for stage 3 of its meaningful use (MU) program for promoting the adoption of healthcare information technology.
March 19, 2015
FDA files MQSA action against NJ imaging center
By
AuntMinnie.com staff writers
The U.S. Food and Drug Administration has filed an adverse event and action report against a New Jersey imaging center.
March 19, 2015
House, Senate introduce SGR repeal bills
By
Kate Madden Yee
Inspired by a joint effort between U.S. House of Representatives Speaker John Boehner and Minority Leader Nancy Pelosi, the House and Senate on March 19 submitted identical bills that would repeal the sustainable growth rate (SGR) formula, according to the Associated Press.
March 18, 2015
FDA voids NY imaging center's MQSA accreditation
By
AuntMinnie.com staff writers
The U.S. Food and Drug Administration has voided the Mammography Quality Standards Act (MQSA) accreditation of a New York City imaging center.
March 18, 2015
CMS opens review of NaF-18 PET payment policy
By
AuntMinnie.com staff writers
The U.S. Centers for Medicare and Medicaid Services (CMS) has opened a review of its reimbursement policy on sodium fluoride F-18 (NaF-18) PET imaging that could result in an end to the requirement that PET facilities collect data when performing the scans.
March 17, 2015
FDA approves VuCOMP's M-Vu CAD 3.2
By
AuntMinnie.com staff writers
Computer-aided detection (CAD) software developer VuCOMP has received U.S. Food and Drug Administration approval for version 3.2 of its M-Vu CAD for mammography software.
March 15, 2015
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