The US Food and Drug Administration is now accepting declarations of conformity to the third edition of the international standard on medical electrical equipment, IEC 60601-1/Ed.3:2006, in support of pre-market submissions1-3. The agency's recognition of the third edition is seen as a significant shift, as the standard focuses more on risk management than pure testing...
Scrip Regulatory Affairs
US FDA recognises AAMI medical electrical equipment standard
11 August 2010
Karen Finn
Not a subscriber ? Request a FREE Trial
Subscribe to Regulatory Affairs Pharma
RELATED CONTENT
NEWS
Scrip Regulatory Affairs News
- NB-MED and BSi attempt to clarify issues over medical electrical equipment standard EN 60601-1:2006
- Key standards committee takes on European Commission objections to EN/ISO 14971
- US FDA consults on human factors testing guidance to improve device safety
- Clinical investigation standard deadline looms as other standards make headway
Other Informa News
ANALYSIS
Regulatory Affairs Pharma Analysis
Other Informa Analysis
EDITORIALS
Regulatory Affairs Pharma Editorials
Other Informa Editorials
FEATURES
Regulatory Affairs Pharma Features
Other Informa Features
COMMENT
Regulatory Affairs Pharma Comment
Other Informa Comments
