US standards group creates glossary of terms for medical device adverse events
This article was originally published in SRA
The US-based standards organisation, the Association for the Advancement of Medical Instrumentation, has created a glossary of terms and suggested meanings related to medical device adverse events1.
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.