We are very proud to introduce our clinical network of 128 clinical sites across Europe, including 18 hospitals, 92 diagnostic centres, 10 laboratories, 8 dental clinics, 1 international patient centre, 1 clinic of cosmetic dermatology, and 1 IVF centre!
We are expanding our cluster of services with a customisable and sustainable approach for the continuous collection of clinical data, which is coming to lift 2 key restraints of manufacturers:
📌access to clinical sites
📌lack of sustainable processes for data collection
The 𝐄𝐯𝐧𝐢𝐚 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐍𝐞𝐭𝐰𝐨𝐫𝐤 guarantees access to diverse populations and the ability to collect device-specific real-world data throughout the lifetime of devices of all types and all risk classes!
The 𝐄𝐯𝐧𝐢𝐚 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐍𝐞𝐭𝐰𝐨𝐫𝐤 can accommodate all types of clinical needs at all stages of clinical development, prioritising the conduct of PMCF activities but also in place to assist with clinical investigations for conformity assessment purposes.
The 𝐄𝐯𝐧𝐢𝐚 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐍𝐞𝐭𝐰𝐨𝐫𝐤 will complement Evnia’s regulatory affairs clinical affairs and medical writing services.
We are now proud to offer a one-stop shop for medtech/ biotech manufacturers: from the development of a regulatory/clinical strategy to its implementation and then towards an holistic approach of life-long post-market surveillance and proactive or retrospective collection of clinical data.
👉 We facilitate market access
👉 We use your device in multiple real-world clinical settings
👉 We generate performance & safety data
👉 We collect those data utilising the Greenlight Guru platform
👉 Our in-house team of regulatory and clinical experts analyse the data leveraging customised data analysis tools
👉 Our in-house team of experienced medical writers prepare/update PMCF and PMS / PSURs and/or peer-reviewed publications to enhance the body of substantiative evidence for your portfolio.
Find out more at 𝐢𝐧𝐟𝐨@𝐞𝐯𝐧𝐢𝐚.𝐝𝐤
𝐖𝐞 𝐒𝐭𝐫𝐢𝐯𝐞, 𝐖𝐞 𝐒𝐞𝐞𝐤, 𝐖𝐞 𝐅𝐢𝐧𝐝. 𝐖𝐞 𝐚𝐫𝐞 𝐄𝐯𝐧𝐢𝐚.
𝐅𝐨𝐫𝐰𝐚𝐫𝐝 𝐓𝐨𝐠𝐞𝐭𝐡𝐞𝐫
