Climedo EU MDR

Digital Health Bites

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: EU MDR

Sascha | Co-Founder & CEO for Climedo, May 27, 2021

MedTech Connect, the Second: Clinical Studies in the Post-Market Phase

Please note that this webinar took place in German.   Recently, our second #MedTechConnect event took place and we were very happy to once again welcome a great number of participants from the MedTech industry to our...

MedTech Connect, the Second: Clinical Studies in the Post-Market Phase
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Marius | Chief Product Officer for Climedo, 07. May 2021

What are the typical phases for manufacturers in a clinical investigation?

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What are the typical phases for manufacturers in a clinical investigation?

Alex | Entrepreneur in Residence for Climedo, 15. April 2021

Survey Results: EU MDR Readiness Check 40 Days before the Deadline

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Survey Results: EU MDR Readiness Check 40 Days before the Deadline

Johann | Sales Executive for Climedo, 25. March 2021

MedTech Connect: Clinical Investigations for Medical Devices

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MedTech Connect: Clinical Investigations for Medical Devices

Tereza | Customer Success Manager for Climedo, 28. January 2021

Myth versus Reality: 4 Common Assumptions about Electronic Data Capture (EDC)

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Myth versus Reality: 4 Common Assumptions about Electronic Data Capture (EDC)

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

Catherine | Marketing Manager for Climedo, 21. December 2020

2020: The Year in Review for MedTech and Climedo Health

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2020: The Year in Review for MedTech and Climedo Health
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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