Newsarchiv
New seminars in the 2nd quarter of 2011
21.03.2011 - ...
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FDA Medical Device User Fee 2010
17.09.2009 - The FDA annual Medical Device User Fee of US$ 2'008.- for the fiscal year 2010 is due between Oct. 1 to Dec. 31, 2009.
We offer to assist you within the re-registration and payment process....
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Italy - Further Deferment of Terms related to the Repertoire until Dec. 31, 2009
03.05.2009 - ...
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Registration of Manufacturer and Medical Devices in Italy
04.03.2009 - ...
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Consolidated Version of MDD 93/42/EEC available
25.03.2008 - After the release of EC-guideline 2007/47/EC in Septembre 2007, the consolidated text of EC-guideline 93/42/EEC are available now and can be downloaded from the EUR-Lex webpage:...
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FDA Unified Registration & Listing System (FURLS)
09.10.2007 - The FDA has implemented significant changes in the registration and listing process of medical device and medical device establishments. Beginning with the new fiscal year (October 1st, 2007) every listed establishment has to use the new FDA Unified Regis...
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Standards Around Sterile Medical Device on the Move
29.03.2007 - Standards around sterile medical devices are in the move.
After a long time without changes, following standards are already or will be replaced soon:...
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