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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
Clinical Trials Regulations | EU vs UK
July 1, 2022
Evnia and Smart-Trial Announce their Strategic Alliance Partnership
March 11, 2022
M.Sc. in Regulatory Writing
February 8, 2022
Evnia ApS announces a new strategic partnership with Myo Health
January 27, 2022
Joint Webinar Evnia-Smart-Trial: PMCF data collection for WET and low-risk Devices
November 5, 2021
Evnia sponsors the 54th Rally-TIF held in Thessaloniki on 9-10 October!
October 2, 2021
Evnia welcomes on board Dr. Maria Maersk!
September 7, 2021
Successful completion of ISO 9001-2015 certification audit!
July 9, 2021
Evnia and SMART-TRIAL team up to tackle the ”clinical data generation” challenge
April 9, 2021
New Interview of Evnia’s CEO at INCUBA
March 16, 2021
QUNIQUE & Evnia Partner To Expand MDR & IVDR Services
January 28, 2021
Evnia is hosting a virtual Roundtable on 3rd February
January 20, 2021
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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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