Clinical Trials & Research

Clinibee's suite of clinical tools empower researchers to focus on insights, not admin.

Clinibee empowers research teams with tools designed in collaboration with clinicians and researchers to enhance efficiency, collaboration, and governance in clinical trials and research.

Our configurable tools ensure accurate, up-to-date information is easily accessible, fostering collaboration while maintaining governance standards.

Whether for patient management, data collection, or post-market surveillance, Clinibee helps researchers focus on impactful insights while addressing key challenges in trial and research processes.

Collage illustration depicting Clinibee's area of expertise

The Problems in
Clinical Trials & Research

Manual workflows—such as in-person data collection, paper forms, and outdated systems— are expensive, hinder efficiency and slow progress.

Clinibee enables participants to enroll and provide consent remotely, reducing administrative overhead and delays.

Identifying suitable participants remains a complex, resource-intensive task, especially in niche or preventive studies

Clinibee simplifies participant identification with configurable, criteria-based flows that can be tailored to specific study aims.

Keeping participants informed, motivated, and involved throughout the study can be a persistent challenge.

Clinibee tracks engagement, retention, and outcomes, improving overall study continuity and success.

Traditional methods often result in incomplete or inconsistent datasets, limiting the potential for actionable insights.

Clinibee provides customisable digital forms for efficient, accurate data collection in real-time.

How Clinibee Solves These Issues

Simplifying Eligibility

Send configurable questionnaires that can be tailored to specific study aims and criteria.

Recording Consent

Clinibee allows participants to enrol in studies/trials and provide consent remotely, all of which can be monitored by the clinical team.

Building Questionnaires

Clinibee allows you to create customisable, digital forms for efficient, accurate data collection in real-time.

Real-Time Analytics

Monitor participant engagement and progress with real-time dashboards and use them to manage the study or trial.

Data Integration

Clinibee can be connected with other systems, consolidating data into a single, easily accessible platform.

Configurable Action Plans

Streamline participant follow-ups with tailored task lists and reminders, ensuring continuity and retention.

Benefits of Clinibee
for Trials & Research

Improved Efficiency

Automate repetitive tasks, freeing up researchers to focus on higher-value activities. Reduce delays in participant onboarding and data collection.

Better Data Collection

Ensures consistent, high-quality data through customisable questionnaires and integration tools. Facilitate comprehensive analysis by consolidating data into a single, user-friendly platform.

Enhanced Patient Engagement

Provide clear communication and action plans, keeping participants informed and motivated, whilst improving retention rates with personalised reminders and follow-ups.

Support for Prevention Efforts

Align with NHS Long Term Plan priorities by supporting research focused on prevention, early detection, and population-level healthcare improvements.

Post-Market Surveillance

Simplify long-term data collection for regulatory compliance and safety monitoring, ensuring continuity beyond trials.

Security and Compliance
You Can Trust

We understand the importance of protecting sensitive clinical data, which is why Clinibee is built with security and compliance at its core.

Data Encryption: All data within Clinibee is encrypted at rest and in transit, safeguarding your content from unauthorised access.
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Role-Based Access Control (RBAC): Access to content is managed through user permissions, ensuring that only authorised personnel can view, edit, or publish clinical guidelines.

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GDPR and NHS DSPT Compliance: Clinibee complies with key data protection regulations, including the General Data Protection Regulation (GDPR) and NHS Data Security and Protection Toolkit (DSPT), so you can trust that your clinical content is managed responsibly and securely.

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Full Audit Trail: Every change to a document is logged, allowing administrators to trace the entire history of each guideline, from draft to publication.

Our platform is designed to meet the highest standards of data protection, ensuring that your clinical content remains secure.

Clinical Trials & Research

Clinibee's suite of clinical tools empower researchers to focus on insights, not admin.

The Problems in
Clinical Trials & Research

How Clinibee Solves These Issues