Use the MedTech virtual platform to contact and network with Repado!
Explore our Software Development & Consultation Services for your new project!
Find more about MedtecLIVE 2020 & MedTech Summit
DMEA goes digital! Join us for a b2b virtual meeting to discuss how our software development services and regulatory consultation can help you with your next project!
Find more about DMEA 2020
Repado contributes in the Covidfight and offers FREE access to its Medical Device Management Platform for ALL Hospital & Research Labs!
Use LTM, to access and support your medical devices, to enable their non-stop performance in the field!
LTM interconnects Manufacturers, Service Professionals and End Users of medical devices under one single application that provides holistic support.
Contact us at myproject@repado.com to set up LTM in your Lab!
Our warmest congratulations to our long term partners at GENOMICA SAU for achieving CE-IVD approval for their diagnostic kits against the COVID-19.
Repado, as GENOMICA’s Software Partner for its CAR® and AUTOCLART® Plus Solutions that use the CLART® technology, is proud and will continue to actively support GENOMICA worldwide in the COVID-19 fight.
CLART® technology used by GENOMICA has the capacity to simultaneously analyze 96 patient samples in less than 5 hours, while the GENOMICA diagnostic kits are highly sensitive and specific in detecting COVID-19, even before the patient shows symptoms!
Boost your liquid handler!
Forget code, Focus on science!
Meet SWIS, the Platform that enables scientists to easily define their protocols via powerful editors! No code required!
A Greek-German cooperation. Stavros Niarchos Foundation Cultural Center Delta Hall | NETWORKING EVENTS
The Hellenic-German Chamber of Commerce and Industry and the Embassy of the Federal Republic of Germany are co-organizing the Innovation Forum: Innovation as a Growth Lead -A Greek-German Cooperation, on November 18, 2019, at the Stavros Niarchos Foundation Cultural Center
Find more about Innovation Forum
Repado is a certified software development house specialized in the Life Science and Healthcare Industry.
With more than 20 years’ experience in the MedTech field, we provide Software Development and Consultation services for regulated environments (MDR/IVDR).
The company is certified under ISO13485:2016 with primary objective the facilitation of harmonized medical device regulatory requirements for Quality Management Systems and ISO9001:2015 Certification for Software development and Implementation.
email: info repado com
