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Our solution

Solving multiple system fatigue

Research advances healthcare, and so should the tools that enable researchers.

We assist Sponsors, CROs and Sites maintain realtime oversight by connecting your existing Data Management systems into one user-friendly interface, as well as provide stand alone focus specific modules so you only use what you need. 

Your Research offers turnkey, modular, and bespoke software solutions across the horizontal participant journey, with simple easy-to-use modules that can integrate with other existing systems if required.

Examples of these include:

  • EDC systems
  • Digital Biomarkers
  • Electronic Health Records
  • Laboratory Information Management Systems 
  • Interactive Response Technology Research

See how Your Research software benefits industry specific roles below.

Participant Recruitment Modules
Benefits for

Participant Engagement

  • Personalised Communication

    Engage participants through automated reminders, personalized messages, and educational materials tailored to their specific needs, improving overall participant experience.

  • Self Visit Scheduling

    Simplify the process of scheduling and rescheduling visits, reducing participant burden and ensuring adherence to protocol requirements.

  • Remote Monitoring

    Leverage tele-health capabilities and remote data collection to minimise in-person visits, providing convenience for participants and potentially expanding trial reach.

  • Empowered Participants

    Provide participants with access to their own data, enabling them to actively contribute to their healthcare journey, fostering a sense of empowerment and engagement.

  • Improved Retention Rates

    By offering a seamless and personalised participant experience, increase retention rates, ensuring a sufficient sample size and data integrity for successful trial outcomes.

Benefits for the

Clinical Research Site

  • Simplified Protocol Execution

    Automate visit scheduling, patient enrolment, and data capture, reducing site burden and enabling efficient trial conduct.

  • Improved Compliance

    Automate data entry, ensuring accurate and complete documentation for compliance with regulatory requirements and audit readiness.

  • Enhanced Participant Engagement

    Leverage automated reminders, personalised communication, and educational materials to improve participant experience, leading to higher retention rates and increased patient satisfaction.

  • Streamlined Site Workflows

    Automate administrative tasks, such as document management and regulatory submissions, reducing administrative burden and allowing sites to focus on patient care.

  • Real-time Support

    Access centralised dashboards and receive real-time guidance and support, facilitating efficient trial conduct and reducing potential delays.

Participant Retention Modules
Participant Retention Modules
Benefits for the

Clinical Research Site

  • Simplified Protocol Execution

    Automate visit scheduling, patient enrolment, and data capture, reducing site burden and enabling efficient trial conduct.

  • Improved Compliance

    Automate data entry, ensuring accurate and complete documentation for compliance with regulatory requirements and audit readiness.

  • Enhanced Participant Engagement

    Leverage automated reminders, personalised communication, and educational materials to improve participant experience, leading to higher retention rates and increased patient satisfaction.

  • Streamlined Site Workflows

    Automate administrative tasks, such as document management and regulatory submissions, reducing administrative burden and allowing sites to focus on patient care.

  • Real-time Support

    Access centralised dashboards and receive real-time guidance and support, facilitating efficient trial conduct and reducing potential delays.

Operations Modules
Benefits for the

Contract Research Organisation (CRO)

  • Improved Collaboration

    Efficiently assign and manage tasks among team members based on expertise, availability, and workload, promoting seamless collaboration and enhanced productivity.

  • Enhanced Data Quality

    Automate data collection, reducing errors and ensuring accurate, reliable data for precise analyses and confident decision-making.

  • Streamlined Site Management

    Centralise communication, streamline site workflows, and provide real-time support to sites, enabling better coordination and faster enrolment.

  • Faster Study Start-Up

    Automate protocol-specific processes, accelerating study start-up activities such as document management, site initiation visits, and regulatory submissions.

  • Enhanced Client Satisfaction

    Deliver high-quality, efficient trial execution to sponsors, leading to increased client satisfaction and potential for repeat business.

  • Competitive Edge

    Stay ahead of competitors by leveraging innovative technology to conduct more efficient and patient-centric trials, attracting sponsors and maintaining a reputation for excellence.

Benefits for

Pharma and Biotech

  • Improved Trial Oversight

    Gain real-time visibility into protocol milestones, enrolment rates, and overall trial progress, allowing sponsors to make data-driven decisions and take proactive actions.

  • Enhanced Efficiency

    Automate protocol execution, data collection, and administrative tasks, reducing manual effort and streamlining trial processes for faster study completion.

  • Cost Savings

    Optimise resource allocation, minimize protocol deviations, and facilitate easier audits, resulting in cost savings throughout the trial lifecycle.

  • Regulatory Compliance

    Ensure adherence to regulatory requirements and industry standards, reducing the risk of compliance issues and supporting successful trial outcomes.

Sponsor
Third Party Integration
Sponsor
Third Party Integration
Benefits for

Pharma and Biotech

  • Improved Trial Oversight

    Gain real-time visibility into protocol milestones, enrolment rates, and overall trial progress, allowing sponsors to make data-driven decisions and take proactive actions.

  • Enhanced Efficiency

    Automate protocol execution, data collection, and administrative tasks, reducing manual effort and streamlining trial processes for faster study completion.

  • Cost Savings

    Optimise resource allocation, minimize protocol deviations, and facilitate easier audits, resulting in cost savings throughout the trial lifecycle.

  • Regulatory Compliance

    Ensure adherence to regulatory requirements and industry standards, reducing the risk of compliance issues and supporting successful trial outcomes.

Participant Retention Modules
Benefits for the

Academia

  • Enhanced Research Efficiency

    Digital clinical trial software streamlines and automates various aspects of the research process, saving time and resources. It allows researchers to efficiently manage data, streamline workflows, automate data analysis, and generate real-time reports. This increased efficiency enables academic researchers to focus more on their core research activities, accelerating the pace of scientific discovery.

  • Enhanced Funding Opportunities

    The adoption of digital clinical trial software demonstrates a commitment to employing innovative research methodologies and cutting-edge technologies. This can increase the attractiveness of research proposals and grant applications, as funding agencies often prioritize projects that leverage digital tools and technologies. By showcasing the use of digital clinical trial software, academic researchers can enhance their chances of securing research funding and support.

  • Increased Data Accessibility for Secondary Research

    Digital clinical trial software facilitates data sharing and provides opportunities for secondary research. Academic researchers can securely store and share de-identified data, making it accessible to other researchers for secondary analysis and further exploration. This promotes knowledge sharing, replication studies, and meta-analyses, fostering a culture of collaboration and advancing scientific understanding.

  • Improved Data Integrity and Compliance

    Digital clinical trial software ensures data integrity by minimizing errors, enhancing data quality, and reducing the risk of data loss. It provides built-in validation checks, data encryption, audit trails, and version control, maintaining the highest standards of data integrity and security. This is crucial for maintaining compliance with regulatory requirements and meeting the ethical standards expected in academic research.

  • Facilitated Collaboration and Multi-centre Trials

    Academic research often involves collaborations between multiple institutions and research centres. Digital clinical trial software provides a centralised platform for seamless collaboration, enabling researchers from different locations to work together effectively. It allows for standardised data collection, centralised study documentation, and real-time data sharing, making it easier to conduct multi-centre trials and promote cross-institutional collaboration.

Let's connect and collaborate

Contact us and we will be happy to show you how Your Research makes a difference in conducting clinical research more efficient and personalized for everyone that is involved.

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