We can design and lead a retrospective and/or prospective study of a selected patient population, comprising of acquisition of real world data from selected healthcare providers as well as accompanying insights from clinicians and patients. At the study design phase, you can choose the population and interesting parameters and research questions. Such study can provide representative, objective data needed for example for discussions with national health authorities. It also opens channels for designing patient support programmes, advocacy and educational activities.
Our services allow a research organization to obtain a 360-degree image of patients selected to participate in publicly reimbursed drug program therapies. It also creates new channels of communication, and the ability to obtain information from medical staff regarding the real-world implementation of the drug program itself. Finally it provides data on the patient’s health condition before, during and after the drug program, which may be crucial in access discussions with payors.
Due to the use of the blockchain technology and our Patient Portal, every patient stays in control of their data and can give or revoke consents whenever they wish from the comfort of their home. We empower patients to be active participants in research studies.
Due to undeniable proof of consent on the blockchain, we’ve got your back in case of any doubt or legal dispute. Our system was created by leading experts in European data and healthcare law such as the GDPR and Data Governance Act.
We are the first entity to build and implement the technological and infrastructural system for pan-European medical data donation, based on the Data Governance Act and European Health Data Space legislation.
Data Lake Application allows you to track the recruitment across different channels. You will know exactly, who recruited how many patients and when. You will be able to easily generate reports and statistics and share it in real time with your study sponsor.