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Home
About
Evnia Group
Corporate Responsibility
Code of conduct
Quality Policy
Ventures
Privacy Policy
Lifecycle Management
Real World Evidence (RWE)
RWE for medical devices
Registries
Clinical Experience Data
PMCF Surveys
Clinical Evaluation Reports
PMCF Plans
Technical Documentation
In-Vitro Diagnostics Regulation (IVDR)
Regulatory Affairs Management
Solutions
Iris
Triad
Authorised Representative
EVA – evnia vigilance algorithm
Management
Resources
Original Publications
News
Industry Insight
Videos
EU Regulations and Guidances for medical devices and IVDs
International Regulations and Guidances
Newsletters
Clients
Careers
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News
The basics of the new In-Vitro Diagnostics Medical Devices Regulation (IVDR)
August 28, 2020
White Paper: State of the Art in the context of the new Medical Device Regulations
August 21, 2020
Designation of the 16th Notified Body under EU-MDR
August 8, 2020
We just got one more successful grant for our subsidiary, OARK (Operating Ark)
July 8, 2020
We are looking for a Biostatistician to join our growing team!
July 8, 2020
State of the Art in EU-MDR /IVDR
June 27, 2020
We Have Completed ISO13485 Training
June 19, 2020
Consolidated EU-MDR Text
May 26, 2020
We Are Hiring a Project Manager. Apply now!
May 25, 2020
Evnia Completes 2 Successful Online Trainings on EU-MDR & Clinical Evaluations
May 2, 2020
Decision on MDR Postponement Published in the Official Journal
April 24, 2020
Evnia Contributes to King’s College COVID-19 Response Fund
April 24, 2020
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HOME
ABOUT
Evnia Group
Corporate Responsibility
SERVICES
Clinical Evaluation Reports
PMCF Planning
Technical Documentation
In-Vitro Diagnostics Regulation (IVDR)
Regulatory Affairs Management
Clinical Experience Data
Ventures
RESOURCES
Original Publications
News
Industry Insight
Videos
CLIENTS
CONTACT
Linkedin
Twitter
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