Investors
VIDA® Diagnostics, a leading developer of quantitative pulmonary imaging software, is supported by revenue, private investment and NIH grants. VIDA received Series A financing in 2007. In December of 2008, VIDA was FDA 510k approved for clinical use in the U.S.
September 2011, the company achieved International Organization for Standardization (ISO 13485) certification and CE certification for its flagship product, Apollo®. The CE certification permits VIDA to sell Apollo for clinical use in the European Economic Area (EEA) and Switzerland. VIDA is currently pursuing CMDCAS certification for regulatory approval in Canada.
For information on investment opportunities, please contact us via email at investors@vidadiagnostics.com or submit our information request form.