Are you a Liquid Handling instrument manufacturer targeting the OEM business?
Do you provide Software Development Kits (SDKs) which require programming knowledge?
Make your customer’s life easier!
Meet SWIS, the Platform that enables scientists to easily define their protocols via powerful editors! No code required!
Meet our team at the Biotechgate Digital Partnering event, designed to support global Business Development in Biotech, Medtech & Pharma.
4 days of digital partnering devoted to new business opportunities for Software development & Consultation on Regulatory affairs.
Find more about Biotechgate Digital Partnering
Join us at the Biotech & Pharma Partnering event to discuss new business opportunities for Software development & Consultation on Regulatory affairs.
Co-organised by the EU-Japan Centre for Industrial Cooperation & the Osaka Prefectural Government, the event is supported by EEN & various Bioclusters from Japan and Europe.
Find more about Biotech ＆ Pharma Virtual Partnering Conference 2020
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!
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
