31.01.2013 – HMA-CAMD Stakeholder Session
IVD Regulation Comments
IVD Regulation Comments Bivda response to MHRA consultation Jan’13 Clinica comment on proposal Jan’13 EDMA…
16.11.2012 – Vigilance WG Meeting
16.11.2012 – Vigilance WG Meeting
14.11.2012 – EUDAMED WG Meeting
14.11.2012 – EUDAMED WG Meeting
06.11.2012 – EAAR Assembly Meeting [Paris, France]
06.11.2012 – EAAR Assembly Meeting [Paris, France] The second assembly meeting in 2012 of the…
18.10.2012 – New & Emerging Technologies WG Meeting
18.10.2012 – New & Emerging Technologies WG Meeting
10.10.2012 – NB MED WG Meeting
10.10.2012 – NB MED WG Meeting
15.06.2012 – Medical Devices Expert Group on Borderline and Classification WG Meeting
15.06.2012 – Medical Devices Expert Group on Borderline and Classification WG Meeting
06.03.2012 – EMA updates guidance on drug/device consultation procedure
EMA updates guidance on drug/device consultation procedure The European Medicines Agency (EMA) has published an…
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…