eCOA driving Erasmus MC’s fully remote MOOD Study
eCOA driving Erasmus MC’s fully remote MOOD Study
Introduction
At Your Research, we’re proud to be supporting the MOOD study led by Erasmus MC in Rotterdam. This innovative...
Discover a fully integrable, modular Clinical Trial Management System
Which adapts to your protocol requirements
That optimises research operations
And improves patient retention
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4,5/5 user reviews
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Our trusted partners
What we do differently
Connect your data throughout the whole participant journey
We develop industry-leading clinical trial software, notably a Clinical Trial Management System (CTMS) and an Electronic Data Capture (EDC) platform.
These modular solutions are crafted based on feedback from researchers, aiming to advance and enhance research processes.
Our innovative solution is termed a “Unified Protocol,” signifying that all operations within the system can be interconnected.
Modules are designed to function independently or seamlessly integrate with your existing EDC or other software, ensuring a smooth flow of pertinent information precisely when needed.
Patient Recruitment
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.
Patient Enrolment
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.
Patient Engagement
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.Â
Our solution
Relevant participant and trial 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 Electronic Data Capture (EDC) software.
Efficient participant recruitment
Experience streamlined processes for participant recruitment and enrollment
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.Â
Improve participant retention
Engage and retain participants
Improve participant retention without adding extra work for study operators by offering personalised experiences and providing ongoing support.Â
Regular communication, incentives, and feedback opportunities can improve engagement while respecting digitalisation limits.Â
Analysing participant feedback and making necessary adjustments can ensure long-term patient engagement success.
Streamline your research operations
Reduce administrative burdens and protocol deviations
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.Â
Reduce paperwork, excel trackers and errors, while improving compliance and efficiency.Â
Focus on delivering quality care and data collection while our system guides you.Â
Seamless integration for improved efficiency
Interconnect your existing systems
We understand the importance of integrating your research systems to streamline your operations.Â
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 usecases
Explore the versatility of Your Research
Our platform streamlines participant recruitment, management, and retention, allowing you to focus on delivering quality care and collecting data.Â
Discover the full potential of your research with our flexible and user-friendly solutions.
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Elevate clinical research
Together
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.Â
Besides this, we offer free online training so you can get the most out of Your Research.
Client support at
Your Research:
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Assistance with the implementation and configuration of the solution
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Protocol design advice based on our extensive experience
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Online training
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Support by phone, e-mail and chat
- Online knowledge base
4.5/5
4,5/5 on app stores
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Revolutionizing research
Delivering best-in-class technology
Your Research is fully compliant with key regulations in clinical trials, ensuring data integrity, privacy and security.Â
Secure Platform
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.
Quality Management
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.
Good Clinical Practice
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.
Medical Device
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.
Let's connect and collaborate
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.