Resourcing and consultancy services
for Contract Research Organisations

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Strategic IT partner services

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BGO Software's services support CROs in their digital transformation by ensuring on-demand premium IT talent for the execution of their projects roadmap or completely outsourcing the development of projects

For 10 years, BGO Software has had the privilege be a trusted IT Service Partner for government and private organisations such as the Health Research Authority (Department of Health in the UK), IQVIA, Covance, Department of Health in Bulgaria. Building a wide range of module-based solutions, platforms and products for our valued clients, presented us with the opportunity to gain in-depth knowledge of the legal and regulatory landscape of the clinical research industry.

Our experience in the adoption of digital health technologies in clinical research help our clients improve patient outcomes collection, streamline the whole clinical research workflow and improve patient engagement.

Our Services

  • Project CTO as a Service

    Single point of contact and technical advisory

    Our tailored consultancy service provides the assistance of an on-demand senior technical leader, that handles the technology-driven challenges, manages the engineering team and drives the project forward for you. CTOaaS delivers immediate value, eliminates operational risks and can foster reusability across the whole company’s strategic roadmap.

  • Managed Dedicated Teams

    The right resources when you need them for as long as you need them

    This service is custom built for large CROs, to provide them with the needed capacity of first class on-demand IT talent wide range of industry related technologies to choose from. Our managed IT services allow our clients to focus on the big picture, architecture design and projects requirements, while we handle the quality of delivery, IT talent management and the relationship with our clients.

Our Portfolio

Clinical Trial Management Systems

We have developed a web-based clinical trial management system, which is 100% modifiable to your organization’s needs while complying with regulatory requirements. Additionally, Clinicubes CTMS can be quickly adapted to facilitate your firm’s schedules, procedures and workflows and it serves as the perfect hybrid between ready-made (“off the shelf software“) and a custom software solution.

  • Full visibility over the costs
  • Meet study timelines
  • End-to-end digital data management
  • Easy reports generation
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Electronic case report form (eCRF)

An electronic case report form is a tool used to facilitate the collection of consistent and valid data from each participating patient in a clinical trial. It accelerates this process, as all patient data (including data from patient questionnaires, and about adverse events) are directly entered into the database. The numerous advantages of eCRF include improved data security and quality, cost-effectiveness, environmental friendliness, and faster but stricter data accessibility and easy analysis.

  • Secure data storage
  • Generate reports in minutes
  • Greater efficiency of study participants
  • Decreased study costs
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Electronic data capture (EDC) systems

For the digitisation of the data collection and management processes of clinical research entities, we have developed a full-featured and customisable Electronic Data Capture (EDC) platform - Metaforms. The platform is an end-to-end module-based solution, which enables you to easily capture and integrate data from various data sources - clinicians, patients, devices, wearables, and EHR systems. Metaforms works seamlessly with other systems, maximises efficiency and patient outcomes and ensures interoperability and industry compliance. Create eCRF, EHR and ePRO documents easily. Ensure the secure data storage and smooth collaboration with electronic documents for your team.

  • Ensure data quality
  • Decrease study duration
  • Database confidentiality and safety
  • Remote access to the data
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Risk-Based Monitoring (RBM) Solutions

Mitigate the risk and improve study quality by implementing advanced risk assessment and monitoring solution. Integrate technology, data analytics and industry know-how to reduce the costs for trial oversight and improve the operations. BGO Software’s risk-based monitoring solution enables you to visualize and manipulate operational data in clinical research. Use predictive analytics to identify and address issues earlier. Еnhance the CRA efficiency and deliver measurable improvements and patient outcomes. With our Risk-Based Monitoring Solutions you can optimize the clinical development models and use data intelligence to reduce risk, while improving study quality and patient safety.

  • Key risk indicators and triggers management
  • Centralized monitoring for increased compliance
  • Predictive and advanced analytics
  • Demonstrated effectiveness across all studies and phases

Trusted by Global Clinical Research Entities

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