Evnia has developed its own vigilance algorithm to support the body of clinical evidence needed for a medical device throughout its lifecycle?
If you are looking for a Medical Device Vigilance Service that will enable the comprehensive collection, assessment, and reporting of vigilance data based on the real-world use of medical devices, we have the right tool!
Whether for benchmarking purposes, international regulatory needs, or the support of clinical and performance evaluations, EVA is here to support your regulatory and clinical journey!
EVA is currently supporting
👉 FDA’s MAUDE, TPLC,
👉 UK’s MHRA Medicines and Healthcare products Regulatory Agency,
👉Germany’s BfArM Bundesinstitut für Arzneimittel und Medizinprodukte, and
👉 Canada’s Health Canada | Santé Canada
but can serve additional databases upon request!