Excited to be attending #ADLM2025! Looking forward to connecting with global laboratory medicine leaders, exploring cutting-edge innovations, and discovering solutions that are shaping the future of clinical diagnostics.
Schedule a meeting with our team and discover how our solutions can support your projects
Our team will be at SLAS Europe to discover the latest Advances in Laboratory Automation, network with industry leaders, and stay ahead of the curve.
Schedule a meeting with our team and discover how our solutions can support your projects
Excited to be visiting Vienna for #ECCMID2025. Looking forward to exploring groundbreaking research, connecting with leading experts, and staying at the forefront of clinical microbiology and infectious diseases innovations.
Schedule a meeting with our team and discover how our solutions can support your research and clinical practice!
The In Vitro Diagnostic Regulation (IVDR) deadlines are rapidly approaching, creating an urgent crisis for medical device software manufacturers. With limited notified bodies and new requirements for stand-alone IVD software, companies must act swiftly to secure certification and maintain EU market access.
We look forward to discover how curiosity fuels innovation and gain valuable insights from
Let's book a meeting and shape the future of medical technology & healthcare together!
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
