> We are an innovative software development & consulting company for the healthcare industry


ISO13485 /2016

repado workflow: innovate - design - develop - consult
medical software development
1

Software
Development

//encoding your needs

Looking for a certified software house to develop your MedTech solution?

  • Medical software (EU MDR/IVDR & FDA)
  • Embedded and control software solutions
  • Software as a Medical Device (SaMD)
  • eHealth / mHealth applications
Consultation on Software Regulatory Affairs
2

Consultation
on Software
Regulatory Affairs

//helping you Understand, Implement
& Conform to Regulatory frameworks
Want to build a new software solution?
We guide you on the regulatory path
Have you already developed your software?
We assist you with the transition to the regulated market (CE/CE IVD)
Not confident your software complies with MDR/IVDR?
We support you in identifying the gaps & achieve compliance

Target Markets

Pharmaceutical
Companies

Med Tech
Companies

Medical Device
Manufacturers

Hospitals /
Laboratories

Our Footprint

We grow together with our customers!

Through our deep expertise and day-to-day involvement in biomedical processes, our customers gain the competitive advantage they need for their target markets.

Using high-quality, consistent and well-engineered technology we are continuously building on new products and advanced services, aiming to further grow our network of customers and strategic partners.

lines

Selected
References

News & Events

SLAS Europe 2025

May 2025

SLAS Europe 2025


Repado will be attending SLAS Europe 2025

read more
ECCMID 2025

March 2025

ECCMID 2025


Repado will be attending ECCMID 2025

read more
IVDR Deadlines Loom: Act Now or Face EU Market Exclusion

February 2025

IVDR Deadlines Loom: Act Now or Face EU Market Exclusion


read more
SLAS USA 2025

January 2025

SLAS USA 2025


Repado's team will be attending SLAS USA 2025 in San Diego

read more
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