Together we improve health
That is where Your Research stands for. To achieve this we engage and work together with patient communities, care and research organizations and other software providers. Supported through an full integrated, open and modulair software suite, we streamline clinical trial or scientific research processes and connect this to clinical practice.
Your Research is a fast growing company that supports streamlining clinical research in order to get new therapies and health solutions faster to the market. Our focus is on transforming processes through implementing innovative software that is guiding participants, researchers and staff. With our experienced team in research and IT we work closely together with our partners and customers in recruiting and/or retention of participants.
ActivityFlow is the enabler of the services behind Your Research Platform. Through this high-end, scalable and smart technology it is possible to organize trials effectively.
Kees van Ooik is co-founder and business director. With his 8+ years of experience on the cutting edge of ICT, healthcare and clinical research he is responsible for the business operation and the strategy.
Peter Tanghe is co-founder and operation director. With his knowlegde and over 12 years of experience by leading teams in the field of information analysis and technology. Peter is responsible for the operations side of the company.
Jan van Deursen is co-founder and technical director of ActivityFlow, the engine behind Your Research. He gained a lot of experience in scalable and high performance software architecture and development the last 7 years. He is also a specialist in machine learning and artificial intelligence.
Compliance is our DNA
Quality and security is the DNA of our operation. That is why Your Research is compliant with various standards in the field of quality management and monitoring, security and privacy, and medical software development.
- ISO 27001 & NEN 7510 certified
- GDPR & HIPAA compliant
- ISO 13485 compliant
- GCP (Good Clinical Practice)
- Medical software development according to ISO-62304
- Medical Device (CE certified)
- GCP compliant
- FDA 21 CFR part 11