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(Mapi Group) An ICON plc Company 13 Mar 18
The Impact of on Economic Operators and - :
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Decomplix Aug 13
The updated rolling plan has just been updated to state that 4 notified bodies have been designated:
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Med-Di-Dia Jul 9
EU What's happening? Is it a 'domino effect'?
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Lean Entries Jun 17
Which one of the can assess the conformity of my ? Take  at to make that match in minutes! Prepare for the new and by checking which Notified Bodies are competent for the task by the current directives.
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Eudamed Jun 6
EC Update - MDCG Q&A on requirements relating to Notified Bodies -
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Elisenda Gendra Oct 22
OMG! Regulation increases workload of EU by 780%, MedTech Europe’s Pirovano tells
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Laurie Mitchell Aug 20
The EC hinted last month that there would be more designations by now. But, we remain at three NBs under the , with several more waiting in pipeline and zero updates to the Nando database. How is industry reacting to this slow progress?
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reuschlaw Mar 29
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MedicalDevicesLegal 3 Oct 14
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PIP Action Campaign Jun 9
Replying to @EU_Commission
+Regulatory authorities are captured, acting in interests of industry, failing patients, particularly women. MEPs insufficiently knowledgeable to reign in out of control manufacturers or private Ltd
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Criterion Edge Aug 2
The European Commission is making headway with 2 more being recommended for designation and a recent surge in published guidances. However, they still face significant pressure with the looming 2020 deadline.
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Gish Consulting LLC Aug 13
Finding I disagree with perspective in this episode. Very member-of-the-club, pining for good ol’ days view—doesn’t account the lazy, semi-competent ethos among that led to issues, the and the NB purge.
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GMED North America Mar 14
Join Florianne Torset and for a discussion on “Enhanced post-market measures & the involvement of in the reporting process” The event takes place on March 19th. Hosted by MassMEDIC and Regulatory and Quality Solutions LLC (R&Q).
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Monir El Azzouzi Aug 22
Awesome game started by @BolleiningerSt and Angelina Hakim. Congrats Ronald Boumans
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MedTech Europe May 15
Salvatore D'Acunto on & "49 applications for MDR and IVDR, already 35 preliminary reports from National Authorities, 27 inspections of which 13 have reached the plan. These are rather encouraging figures."
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Jose Saenz Jun 5
Looking forward to the next week, to talk about and the concepts of and and how they relate to , and in the .
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Swedish Medtech 21 Mar 18
Ana Burgos from describes the process for the joint assessment & designation of .
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Decomplix Aug 20
These are the four notified bodies designated under the new EU Medical Device Regulation
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M. Dræbye Gantzhorn Nov 1
EU marketing authorisation holders may have to fight over dwindling capacity of notified bodies...
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Malin Hollmark 21 Mar 18
Ana Burgos on the joint assessment of . 60 assessment for & 45 for in 22 months! Phew...
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