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Medical Device Technology|July 9, 2008
Who owns the 510(k)?Maria E Donawa
Medical Device Technology|October 27, 2009
New European guidance on borderline productsMaria E Donawa,
Medical Device Technology|June 18, 2002
The IVD directive: planning for complianceMaria E Donawa
Medical Device Technology|May 31, 2003
IVD authorized representativesMaria E Donawa
Medical Device Technology|August 3, 2004
The essential element of ethicsMaria E Donawa
Medical Device Technology|May 25, 2004
Guidance on submitting quality system informationMaria E Donawa
Medical Device Technology|December 20, 2003
FDA pilot programme in support of global harmonisationMaria E Donawa
Medical Device Technology|July 16, 2002
Implementation of the medical device directives in ItalyMaria E Donawa
Medical Device Technology|January 13, 2009
The evolving process of European combination product review, Part IIMaria E Donawa
Medical Device Technology|November 8, 2008
The evolving process of European combination product review, Part IMaria E Donawa
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