BAYOOMED – We develop medical apps
BAYOOMED is specialized in the development of medical apps and medical (standalone) software. With more than 250 person years of project experience in software development in the regulated medical and pharmaceutical environment and over 800 medical & pharma customers, we are among the most experienced medical software developers in Europe.
We engineer MHEALTH / EHEALTH applications under iOS (iPhone & iPAD) and Android according to IEC 62304 and support product developers and innovators from the pharmaceutical and medical technology sectors in all phases of software product lifecycle. We have experience in software engineering in the medical device classes I - III and the software security classes A - C.
BAYOOMED is highly professional in the regulated CE & FDA environment. We design, develop, test, validate and document medical software and medical apps in accordance with the regulatory standards IEC 62304, ISO 14971, IEC 62366 as well as the FDA Guidance for Mobile Medical Applications. We offer Due Dilligence Services for medical device classifications, usability engineering, risk management, technical documentation and FDA and CE registration.
Our Quality Management processes certified by TÜV Hessen according to ISO 13485 are an evidence to our passion for sustainable solutions and distinct customer focus.
Our customers have been entrusting us with their sensitive projects for more than 18 years. Repeated orders at a rate of over 96%, multiple awards for outstanding development support and a high recommendation rate incent and motivate us to support each new customer with our best services.
We engineer MHEALTH / EHEALTH applications under iOS (iPhone & iPAD) and Android according to IEC 62304 and support product developers and innovators from the pharmaceutical and medical technology sectors in all phases of software product lifecycle. We have experience in software engineering in the medical device classes I - III and the software security classes A - C.
BAYOOMED is highly professional in the regulated CE & FDA environment. We design, develop, test, validate and document medical software and medical apps in accordance with the regulatory standards IEC 62304, ISO 14971, IEC 62366 as well as the FDA Guidance for Mobile Medical Applications. We offer Due Dilligence Services for medical device classifications, usability engineering, risk management, technical documentation and FDA and CE registration.
Our Quality Management processes certified by TÜV Hessen according to ISO 13485 are an evidence to our passion for sustainable solutions and distinct customer focus.
Our customers have been entrusting us with their sensitive projects for more than 18 years. Repeated orders at a rate of over 96%, multiple awards for outstanding development support and a high recommendation rate incent and motivate us to support each new customer with our best services.