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!
We look forward to connect with international experts from the medical industry
Let's book a meeting and shape the future of medical technology & healthcare together!
We look forward to connect with the global laboratory medicine community
Let's book a meeting and shape the future of medicine together!
The voice of our customers: Certest. SWIS™ software is transforming molecular diagnostics at Certest Biotec by automating processes that significantly improve efficiency and accuracy in laboratory workflows.
Heading to Barcelona for SLAS Europe 2024. Ready to dive into cutting-edge lab automation & biotech innovation, and forge new connections.
Let's connect!
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
