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.