| NSAI
is holding a Medical Devices Information
Day on the recent revisions to the Medical
Devices Directive (MDD 2007/47/EC), concentrating
on the extra regulatory demands on Notified
Bodies and Manufacturers.
Manufacturers need strong partnerships
with a Notified Body that has the expertise
and is adaptive, resourceful, responsive
and capable of facilitating timely CE
Mark approvals.
NSAI has this ability and fully embraces
current regulatory challenges to expand
Ireland’s competitive edge.
The Information Day provides an opportunity
to highlight the ‘public good’
and national importance of NSAI working
closely with the medical device industry,
the IMDA, IDA, Enterprise Ireland, IMB
and medical professionals. |
