Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maria Donawa

Showing results (21-30 of 50) with videos related to

Pageof 5
Sort By:
Medical Device Technology|April 14, 2006
US guidance on formatting 510(k)sMaria Donawa
Medical Device Technology|August 12, 2004
Effective risk management programmesMaria Donawa
Medical Device Technology|July 17, 2004
Beyond the US submisson processMaria Donawa
Medical Device Technology|December 14, 2007
Implementing new European vigilance proceduresMaria Donawa
Medical Device Technology|March 20, 2008
Scope of the European Medical Device DirectivesMaria Donawa
Medical Device Technology|October 8, 2003
Managing changes during a clinical investigation, Part IMaria Donawa
Medical Device Technology|November 2, 2005
Understanding US labelling requirementsMaria Donawa
Medical Device Technology|October 18, 2005
Successful recruitment for medical device clinical studiesMaria Donawa
Medical Device Technology|October 26, 2002
Update on the forthcoming European Clinical Investigation StandardsMaria Donawa
Medical Device Technology|May 28, 2002
FDA final guidance on software validationMaria Donawa
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Medical Device Technology|April 14, 2006
US guidance on formatting 510(k)sMaria Donawa
Medical Device Technology|August 12, 2004
Effective risk management programmesMaria Donawa
Medical Device Technology|July 17, 2004
Beyond the US submisson processMaria Donawa
Medical Device Technology|December 14, 2007
Implementing new European vigilance proceduresMaria Donawa
Medical Device Technology|March 20, 2008
Scope of the European Medical Device DirectivesMaria Donawa
Medical Device Technology|October 8, 2003
Managing changes during a clinical investigation, Part IMaria Donawa
Medical Device Technology|November 2, 2005
Understanding US labelling requirementsMaria Donawa
Medical Device Technology|October 18, 2005
Successful recruitment for medical device clinical studiesMaria Donawa
Medical Device Technology|October 26, 2002
Update on the forthcoming European Clinical Investigation StandardsMaria Donawa
Medical Device Technology|May 28, 2002
FDA final guidance on software validationMaria Donawa
Pageof 5