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About
Evnia Group
Corporate Responsibility
Code of conduct
Quality Policy
Ventures
Services
Real World Evidence (RWE)
RWE for medical devices
Registries
Clinical Experience Data
PMCF Surveys
Clinical Evaluation Reports
PMCF Planning
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
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EU Regulations and Guidances for medical devices and IVDs
International Regulations and Guidances
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Antarctica – Evnia expedition for awareness and science
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Filotimo and Evnia
August 23, 2023
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Evnia – Rally – Harmony in human/device interplay towards Excellence
May 9, 2023
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Evnia – Regulatory & Clinical
March 17, 2023
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OARK betahealth
August 12, 2022
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OARK
September 22, 2021
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Evnia – Corporate Responsibility
July 8, 2020
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EU/MDR, 1 Year Extension – No Time To Lose
April 24, 2020
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Evnia – A Name With Much More In It
March 31, 2020
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ABOUT
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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
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Twitter
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