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

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