Climedo Notified Bodies

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In unserem Blog finden Sie Trends und Neuigkeiten rund um MedTech, EU-MDR, klinische Studien und Digital Health und bleiben Sie bei Änderungen regulatorischer Anforderungen immer auf dem aktuellsten Stand.

Category: Notified Bodies

Catherine | Marketing Manager for Climedo, August 10, 2021

Complete list of IVDR certified Notified Bodies

For the verification of the essential requirements for in vitro diagnostic medical devices, manufacturers must follow the IVDR as well as its conformity assessment procedures. For this purpose, Notified Bodies must be involved with the...

Complete list of IVDR certified Notified Bodies
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Veronika | Co-Founder & COO for Climedo, 05. January 2021

Virtual Audits under EU MDR – What You Need to Know

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Virtual Audits under EU MDR – What You Need to Know

Sascha | Co-Founder & CEO for Climedo, 05. December 2020

First EUDAMED Module Live – Here’s What You Need to Know

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First EUDAMED Module Live – Here’s What You Need to Know

Marius | Chief Product Officer for Climedo, 12. October 2020

Medical Devices 101 // Dental Implants

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Medical Devices 101 // Dental Implants

Sascha | Co-Founder & CEO for Climedo, 01. October 2020

Complete List of MDR-certified Notified Bodies

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Complete List of MDR-certified Notified Bodies

Sascha | Co-Founder & CEO for Climedo, 08. July 2020

How to know if your product is a medical device

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How to know if your product is a medical device

Sascha | Co-Founder & CEO for Climedo, 28. May 2020

Recap of our EU MDR Webinar on May 26, 2020

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Recap of our EU MDR Webinar on May 26, 2020
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CLIMEDO IN THE NEWS

Outsourcing-Pharma: Survey: research industry keen on DCT benefits, slow to adopt Outsourcing-Pharma: Survey seeks to chart adoption of decentralized trials, future plans RAPS: Challenges and opportunities in medical device clinical trials in Europe CenterWatch: European Trials Lag Behind U.S. in Decentralization, Survey Finds Outsourcing-Pharma: Report reveals obstacles to implementing digital trial tech Healthcare Global: A guide to labelling compliance for medical devices Easy Medical Device: EU MDR Survey: What is the Industry’s opinion? RAPS: EU MDR Countdown: Readiness of medtech companies in Europe EPR: How small medical device manufacturers can achieve cost-effective compliant labelling MedTech Dive: EU MDR delay has not made new rules easier to stomach: exec poll RAPS: EU MDR survey: Time investment, costs, and personnel resources Easy Medical Device: What is the cost of an EU MDR project? Podcast: What is the true cost of the EU MDR? MedTech Insight: EU MDR Compliance Will Cost More Than 5% Of Revenues For Half Of Medtechs, Survey Says MedTechDive: EU MDR costing smaller medtechs 5% of their annual sales: survey Zollhof: Climedo’s digital symptom diary supported by Germany’s Federal Ministry of Health Helping MedTech companies comply with EU MDR: A case study Climedo Named Winner of EIT Health’s Headstart Program Medical Plastics News: How Covid-19 is impacting the medtech industry Survey results suggest medtech companies are not ready for EU MDR EIT Health: COVID-19 – Response from EIT Health Germany community