Implementing eConsent
Supporting Diverse Processes for Optimal Patient Retention and Operational Support
Electronic consent (eConsent) technology is not a new concept and has been used successfully in...
Empowering Clinical Trials through a Unified Protocol
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 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
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.
Consent
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.
Optimise
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.
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 (EDC) software.
Efficient participant recruitment
Experience streamlined processes for participant recruitment
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
Engage and retain participants
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.
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.
Reduce paperwork, excel trackers and errors, while improving compliance and efficiency.
Focus on delivering quality care and data collection while our system guides you.
Seamless integration for improved efficiency
Interconnect your existing systems
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 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.
Discover the full potential of your research with our flexible and user-friendly solutions.
Solving Re-Consent
Enhancing Clinical Trials Through Re-Consent:
The Digital Revolution
Introduction
Clinical trials are the cornerstone of medical research, paving the way for groundbreaking...
News update: ECRAID and Your Research collaboration
Press Release 12/09/2023:
Ecraid and Your Research announce strategic collaboration to enhance clinical research network across Europe
Ecraid, a pan-European clinical research...
Paper versus Electronic Consent: A side-by-side comparison
Overview: Paper consent vs. eConsent
Here we examine the differences between traditional paper-based consent forms to electronic consent. As technology continues to shape the way...
Real Solutions 4 part series – Ep 1: Participant Burden
Overview
We recently polled your thoughts on our LinkedIn page and the results are displayed in the graph.Over the coming weeks, we will offer you our insight gained from...
The Clinical Trial Unit Planner (CTUP) module
The Clinical Trial Unit Planner (CTUP) module from Your Research is new software making daily complex clinical planning a breeze.
Why the CTUP
Retain a firm grasp on all study...
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.
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.
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.