๐— ๐—ฒ๐—ฑ๐—ถ๐—ฐ๐—ฎ๐—น ๐——๐—ฒ๐˜ƒ๐—ถ๐—ฐ๐—ฒ ๐—Ÿ๐—ถ๐—ณ๐—ฒ ๐—–๐˜†๐—ฐ๐—น๐—ฒ ๐— ๐—ฎ๐—ป๐—ฎ๐—ด๐—ฒ๐—บ๐—ฒ๐—ป๐˜ ๐—ฆ๐—ฒ๐—ฟ๐˜ƒ๐—ถ๐—ฐ๐—ฒ๐˜€ ๐—ฏ๐˜† ๐—˜๐˜ƒ๐—ป๐—ถ๐—ฎ : ๐˜๐—ต๐—ฒ ๐—ฆ๐—ฒ๐—ฟ๐˜ƒ๐—ถ๐—ฐ๐—ฒ ๐—ผ๐—ณ ๐—ฃ๐— ๐—–๐—™ ๐—ฆ๐˜‚๐—ฟ๐˜ƒ๐—ฒ๐˜†๐˜€

Evnia is a pioneer in the design and conduct of PMCF Surveys and has been supporting the postmarket surveillance and PMCF programs of MedTech manufacturers with sustainable, streamlined solutions that enable the use of data from PMCF Surveys to
๐Ÿ“substantiate claims
๐Ÿ“ frame the intended medical field of a medical device
๐Ÿ“ identify and understand off-label uses
๐Ÿ“ update/optimise device design
๐Ÿ“provide input for new product development

Our strengths?
๐Ÿ“ Holistic approach and critical gap assessment for the identification and weighing of clinical data gaps and the justification of PMCF needs
๐Ÿ“ In-house multidisciplinary expertise
๐Ÿ“ Standardised processes and templates
๐Ÿ“ Pan-european clinical network with access to diverse populations and the ability to collect both prospective and retrospective clinical data

Read more in our dedicated brochure

If you are looking for optimised lifecycle management activities and to maximise your post-approval market status, we have the right program!
Let our team of experts accommodate your quality and regulatory journey!

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