Evnia provides the Medical Device, Pharma and Biotech industries with specialised consulting services in the areas of Regulatory Affairs/Compliance, R&D and Management by transforming data and regulations into measurable actions and tailored solutions. 

Key know-how and services include:
- Clinical Evaluation Reports 
- Clinical and Technical Documentation
- In Vitro Diagnostics (IVDR), Performance evaluation Plans/reports (PEP/PERs) 
- Regulatory and Project Management and external sourcing activities
- Regulatory Compliance for Authorities globally
- Clinical Experience Data

We serve the Life-Sciences Industry and promote patient care and quality of life by striving, seeking and finding solutions that support compliance and R&D decisions in investments, innovation and medical/regulatory communications. 


Biotechnology

Medical Devices

Pharmaceutical

Evnia

Evnia's headquarters in København, Denmark

Dr. Efstathios Vassiliadis

Maria Maersk

Angeliki Koukoura

Martina Pollastrini

Giannis Mylopoulos

Chris Busse

This department specializes in creating and managing regulatory and clinical documents for the healthcare sector.

Evnia

Org chart

Teams

Medical Writing

Offices

Evnia

Org chart

Teams

Medical Writing

Offices

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