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We develop industry leading clinical trial software modules from researcher led feedback that advance and enhance research, notably along the participant trial journey.
Our unique solution is defined as a “Unified Protocol” meaning all operation can be connected.
Modules can stand alone, or integrate with your existing EDC or other software to provide a seamless flow of relevant information at the right time.
Recruit the right participants via advertisement or a pre-existing database.
Let them register, pre-screen and schedule an in-person, video- or phone call visit themselves.
Inform participants about an in-person or digital study.
Test their knowledge and willingness to participate ensuring motivated participants enrol preventing drop-outs later.
Sign the ICF with an electronic signature.
Receive guiding through scheduled automation of protocol activities and visits, to prevent administrative burdens and possible protocol deviations.
Easily keep participants engaged via a mobile app.
Plan study visits based on resource availability and protocol schema, and capture relevant data at the right time.
We created an open and end-to-end Unified Protocol platform that assists you the researcher engage and retain participants by automating your clinician and participant tasks in one safe and secure online environment which can integrate with other (EDC) software.
Streamline your recruitment process with automated pre-screening and instant appointment scheduling.
Enhance the experience for both participants and researchers, ensuring higher participant retention rates and less manual administrative activities leading to a more enjoyable clinician experience.
Improve participant retention without adding extra work for study operators by offering personalised experiences and providing ongoing support.
Regular communication, incentives, and feedback opportunities can improve engagement while respecting digitalisation limits.
Analysing participant feedback and making necessary adjustments can ensure long-term patient engagement success.
Prevent administrative burdens and protocol deviations for study teams/sites with our streamlined participant and data management system that offers protocol automation and workflow support.
Reduce paperwork, excel trackers and errors, while improving compliance and efficiency.
Focus on delivering quality care and data collection while our system guides you.
We understand the importance of integrating your research systems to streamline your operations.
Our flexible platform, we identify as a Unified Protocol, supports data exchange through our Application Programming Interface (API) and other methods, ensuring compatibility and continuity across your research processes.
Our platform streamlines participant recruitment, management, and retention, allowing you to focus on delivering quality care and collecting data.
Discover the full potential of your research with our flexible and user-friendly solutions.
Your Research is renowned for its support team that puts clients, partners and their participants first.
We help every study team to maximise the use of the solution and provide individual support by phone, email, and chat.
Besides this, we offer free online training so you can get the most out of Your Research.
Client support at
Your Research:
4,5/5 on app stores
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Your Research is fully compliant with key regulations in clinical trials, ensuring data integrity, privacy and security.
Our organization is ISO-27001 certified and fully compliant with GDPR and HIPAA regulations. Implementing your privacy policy is made easy with our solution, allowing you to focus on delivering quality care and data collection with peace of mind.
Delivering quality is our top priority, which is why we have implemented a quality management system in accordance with ISO13485, an extension of ISO9001. This ensures that our products and services meet the highest quality standards, providing you with a reliable and effective solution for your research needs.
Our commitment to Good Clinical Practice (GCP) underscores our focus on quality, ethics, and compliance. This standard ensures that we adhere to strict guidelines and regulations to protect participants and ensure data integrity.
Our medical expert rules engine adheres to rigorous Medical Device regulations and guidelines, guaranteeing exceptional data quality and integrity. This certification showcases our dedication to providing a trustworthy and compliant platform for your research requirements.
Contact us, and we would be delighted to demonstrate how Your Research can significantly impact the conduction of clinical research by enhancing efficiency and personalisation for all stakeholders involved.
