Leveraging clinical data for the smart evolution of medicine.
Experience true interoperability in action with our digital ecosystem.
We develop digital health innovations that transform your company into a learning enterprise. A unique semantic layer enables full medical data interoperability and opens a new world of data quality, flexibility, and real-world evidence.
With our integrated medical informatics, clinical trial, medical device and real-world data collection ecosystem of services and solutions, we will take you through the entire transformation process and empower people, processes, and progress.
Advance your workflow with actionable insights, and achieve better patient outcomes.
As medical professionals, data scientists, and information technology specialists, we support the development of personalized treatments and improve patient well-being.
Accelerate and simplify the complex processes of clinical trial data management and analysis.
We ensure you get the most out of your clinical trial data. From data collection, standardization, and storage, through to appropriate statistical analysis and interpretation, all the way to the final statistical analysis report.
Fast track your medical device market authorization by evaluating the safety and performance in full compliance with regulatory requirements such as the EU MDR. The features of our software ecosystem have you covered when compiling your technical files for device design, pursuing a CE mark, capturing clinical data, developing connectivity solutions, and performing post-market surveillance.
Empower your analytics with the best data available and gain relevant evidence and meaningful insights.
We support you by collecting fully machine readable, OMOP and CDISC compliant data within a global network of experienced clinical data professionals and offer you broad and diverse patient population for your studies.
We take pride in our clients’ satisfaction.
Their dedication to, and support of, our projects has resulted in clear quality deliverables. They are always there to answer any questions with expertise in a timely manner. I am looking forward to our next project together.
Wemedoo’s contribution was essential in creating the Smart Oncology project for our Foundation. I am very enthusiastic about our collaboration and especially impressed about the depth of knowledge, assistance and advice they provide. Their expertise and dedication are exquisite, result-oriented and on a very high, professional level.
All jobs, both large and small, are performed with the same dedication to quality, detail, innovative thinking, and rigor. It is always a pleasure to work with the Wemedoo team.
Wemedoo embodies all the traits desired in a partner in the clinical trial industry - expertise, innovation, reliability, compliance, and attention to detail.
We are a proud member of leading industry organizations in Europe and the US...
…and implement the highest industry standards.
It is a commitment to constantly learn, improve, and evolve through quality.
Our Latest Thinking. View All
11 May 2022Automating Stock and Supply Through RTSM
09 Mar 2022The Coupling of RTSM and the eCRF
01 Feb 2022Why Are Electronic Health Records Error-Prone?
10 Feb 2021Adverse Reaction Terminology: MedDRA and WHO-ART
05 Jan 2021EHR to EDC: The Benefits of Direct Sourcing