US FDA investigates CT imaging quality assurance programmes
This article was originally published in SRA
The US Food and Drug Administration is investigating whether radiation overexposures that occurred during CT brain perfusion scans at an unnamed healthcare facility reflect a more widespread problem with CT quality assurance programmes1.
You may also be interested in...
An ambitious action plan drawn by an EU task force, if implemented on a priority basis by the European Commission, could increase the EU’s capacity to advise on, assess and analyze big data.
Swissmedic will scale back its review procedure for certain anti-infectives if the indications for which approval is being sought are identical to those approved in the EU or the US.
Based on the operational experience gained using the new international standard for reporting suspected adverse reactions in EudraVigilance, the EU has decided to set a date for its mandatory use.