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  • Solutions
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      • eCRF: Electronic Case Report Form
      • eSource
    • Streamline Operations
      • Visit Planner
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      • Protocol and Workflow Automation
    • Third Party Integrations
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      • Medical Devices & Wearables
      • Application Specific Systems
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    • eCOA: Electronic Clinical Outcome Assessment
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Empowering Clinical Trials through a Unified Protocol

Which adapts to your protocol requirements
That optimises research operations
And improves patient retention
Request information

* * * * *
4,5/5 user reviews
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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. 

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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.

  • Flexible

    Set-up your study fast on a system that adapts to suit your protocol requirements, not the other way around.

  • Modular

    Utilise just what you need. Use interchangeable modules depending on your specific study requirements and gain confidence with minimal risk.

  • Integrable

    Connect your current EDC or data collection system, device or other sources via our standardised 'off the shelf 'API.

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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. 

-> Find out more

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.

-> Find out more

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. 

-> Find out more

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.

-> Find out more

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.

Use CasesVisit Scheduling

Solving the Challenges of Clinical Trial Flow, Data Management and Resource Planning

Solving the Challenges of Clinical Trial Flow, Data Management and Resource Planning with One solution Introduction Clinical research plays a pivotal role in advancing medical...
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eConsentUse Cases

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...
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eConsentUse Cases

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...
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ArticlesNews

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...
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eConsentUse Cases

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...
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ePROUse Cases

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...
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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. 

Besides this, we offer free online training so you can get the most out of Your Research.

Client support at
Your Research:

  • Assistance with the implementation and configuration of the solution
  • Protocol design advice based on our extensive experience
  • Online training
  • Support by phone, e-mail and chat
  • Online knowledge base
 4.5/5

4,5/5 on app stores
-> Read more

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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. 

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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.

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