Medical device
Do you want to develop Software as a Medical Device?
We can do the project together.
Check our approach to developing medical software that matches regulations and clinical workflow.
Medical device software development – our offer
Compliance with technological and medical regulations
Development of a project compliant with your idea but also with technological and medical regulations as well as best practices. Our multidisciplinary team consisting of engineers, bioengineers, scientists and clinicians ensures that the goals of your project is met.
Documentation creation
During the software development process we create documentation that supports and speeds up the certification process of your solution. Thanks to our experience, by developing a project with us, you will receive professional documentation. We are able to develop Software as a Medical Device tailored to the client’s needs.
Assistance within the software development lifecycle
Assistance within the whole software development lifecycle, whether your in pre-project, feasibility, proof of concept or development phase. We can also help you with maintenance when the project is done and your product is ready.
Experienced team in building up medical device software
Experience. We were involved in the development of certified medical devices that have successfully are implemented in clinical workflow and are used in practice.
Our knowledge of the ISO 14971 standard and the ability to create healthcare software systems while complying with the IEC 62304 standard will ensure the relevant certification you may require.
We work according to our own Quality Management System. Every process we have implemented internally and our work approach are quality-based.
Our internal QMS meets the ISO 13485 standard. We are experienced practitioners in the development of medical software that meet the requirements of this standard. Our competences support client’s certification process.
We have experience in software development compliant with CE and FDA.
Experienced team in building up medical device software
Experience. We were involved in the development of certified medical devices that have successfully are implemented in clinical workflow and are used in practice.
Our knowledge of the ISO 14971 standard and the ability to create healthcare software systems while complying with the IEC 62304 standard will ensure the relevant certification you may require.
We work according to our own Quality Management System. Every process we have implemented internally and our work approach are quality-based.
Our internal QMS meets the ISO 13485 standard. We are experienced practitioners in the development of medical software that meet the requirements of this standard. Our competences support client’s certification process.
We have experience in software development compliant with CE and FDA.
Learn more about our competences
Let’s work on your challenges together!
Contact us:
Let’s work on your challenges together!
Contact us:
