Menu
Search
Home
People
Our expertise
Publications
Events
Careers
Get in touch
standardisation
Article
Software as medical device – regulatory requirements, product liability
15 Nov 2010
,
Erik Vollebregt
I attended an interesting seminar today about software as medical device organised by NEN, the Dutch standardisation institute. Speakers at the seminar highlighted the different views on this subject from the perspective…
Read more
Navigate through our knowledgebase
advertising
apps
authorised representative
Borderline
business compliance
CE Mark
CE marking
Clinical evaluation
Clinical investigation
Clinical Trials
Cybersecurity
Data Protection
eHealth
enforcement
ENVI
Eucomed
Eudamed
food
health
health claims
In vitro diagnostics
information
IVD
IVDR
ivds
labelling
Liese
market surveillance
MDR
MEDDEV
Medical devices
mhealth
Notified Bodies
notified body
Novel Food
nutrition claims
personal data
PMA
PMS
privacy
Quality system
Recast
reprocessing
revision
Roth-Behrendt
Software
standards
technology
UDI
Unannounced audits