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Gish Consulting LLC Dec 10
Voluntary actor registration (for EOs) under EUDAMED will begin May 2020 allowing acquisition of the SRN needed to make vigilance reports under . Thanks to DG SANTE, this good news may help ease the expected backlog for competent authority (CA) validations.
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TUV Rheinland NA Dec 10
As the application date quickly approaches, we have received many questions regarding the new regulation. To help our customers, our experts have compiled & answered the most frequently asked questions into one convenient document:
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tracekey solutions GmbH 12h
"You better find a way to track and keep data that should have been going into Eudamed from the start because it is likely that you’ll need to upload it retrospectively when Eudamed goes live..." ->
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Tony Knobloch 9h
Sign up for this GT webcast which will discuss items to consider on your / readiness checklist & how to navigate your remediation efforts.
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Atos Syntel 2h
With deep experience in medical devices and diagnostics, we can help make a smooth transition to compliance. To learn more, visit
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Network Partners Dec 5
The second Corrigendum to the European Union Medical Device Regulations (EU MDR) (2017/745) has been published by the Council of the European Union. What does this mean for your medical device? Learn more here -
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TUV Rheinland NA Dec 5
The new will bring forth many new requirements for medical device manufacturers. As such, many questions have surfaced regarding these new changes. Interested in learning more? Check out our informative FAQ on the new EU MDR!
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RegDesk, Inc. 7h
Under new EU MDR regulations, there are more devices than ever that require notified body review but there may be a shortage of firms to handle the incoming workload.
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Freyr Solutions Dec 5
The countdown for has already begun. How close are you in aligning with the new requirements? Make no delay for compliant transition. Consult.
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Network Partners Dec 9
The Eudamed database requires submission of information for public and restricted sites. Download your Eudamed white paper today and contact Network Partners' labeling team for EU MDR support -
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Easy Medical Device 13h
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Gish Consulting LLC Dec 6
news piece worth retweeting regarding grace period changes.
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Network Partners Dec 3
Network Partners' labeling team supports medical device clients to obtain compliance in all facets of their EU MDR planning, including the understanding of Eudamed. Download your Eudamed white paper today -
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Monir El Azzouzi 8h
MDR Current state with @BolleiningerSt from be-on-Quality GmbH
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Amanda Maxwell Dec 9
European Commission has told Council of EU that 700 people have applied to be on the expert panels. This is good news and more than double what is needed.
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Monir El Azzouzi 14h
This week I am releasing on my youtube channel the presentation made by @BolleiningerSt from be-on-Quality GmbH ar MDR State of Play by Stefan Bolleininger (MEDICA COMPAMED 2019)
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Climedo Health Dec 3
How the Will Shape the Future of : Brand-new Playbook with an industry outlook and tips on how to use the MDR as a powerful lever for growth.
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MedicalDevicesLegal Dec 10
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VISTAAR Dec 4
May 2020 is right at the corner and the are long released. Don’t fall behind when summarize is there. Get all the latest updates and on . Be ready to enter the updated market. Make a fresh start. Know more at
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Peter Kits 16h
A bumpy road. But we’ll get there. Collaborating and sharing experiences is pivotal. If you are not convinced that a good working MDR is important please watch Bleeding Edge
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