IMDRF-MC X – National Competent Authority Report Exchange Programme
Borderline and Classification Documents From The Commission
Borderline and Classification Documents
26.10.2015 – EU Medtech Reform Proposals May Jeopardize Authorized Representatives
26 October 2015 – EU Medtech Reform Proposals May Jeopardize Authorized Representatives; Exacerbate ‘Ghost’ Problem…
03.02.2012 – Guidance on EU Authorised Representatives published
03.02.2012 – Guidance on EU Authorised Representatives published The European Commission has published MEDDEV 2.5/10 ‘Guideline…
30.01.2012 – European Commission publishes several new guidance documents
30.01.2012 – European Commission publishes several new guidance documents The European Commission has recently published…
19.01.2012 – Revised MEDDEV on post-market clinical follow-up studies published
19.01.2012 – Revised MEDDEV on post-market clinical follow-up studies published The European Commission has published…