Managed EDC and Statistical Services Services for Research Studies

EDC, automated TFLs and automated analysis in one platform

From eCRF programming and validation checks to dashboards, conditional notifications and final data delivery, our team handles the technical database work so your researchers can concentrate on running the study.

We work with CROs, research organisations, universities, healthcare teams, medical-device companies and other organisations that need a dependable data-capture system without keeping an internal programming team.

Discuss your study

Trusted and used by leading pharmaceutical companies

Eight study types we support:

Interventional, clinical and experimental research

Structured screening, scheduled assessments and controlled data collection for interventional and experimental studies.

We translate your approved questionnaire, protocol requirements and data specifications into a study-ready electronic Case Report Form.

Every study follows an agreed process covering specification, programming, quality control, User Acceptance Testing, activation and live change control.

A study coordinator enters visit data on a tablet while a participant waits

Your database can support

  • Participant screening and eligibility assessment
  • Study enrolment
  • Visit schedules and follow-up assessments
  • Intervention allocation fields
  • Baseline and outcome measurements
  • Adverse-event and safety-related questions
  • Protocol-deviation recording
  • Conditional safety notifications
  • Data validation and edit checks
  • Investigator review and electronic sign-off
  • Controlled database closure and data delivery
Observational and cohort studies

Consistent data across prospective, retrospective, cross-sectional, case-control and longitudinal research.

We configure databases for multiple study visits, repeated assessments, participant follow-up and long-term outcome monitoring.

Conditional logic shows participants and researchers only the questions relevant to them, which reduces unnecessary data entry and improves completion.

Depending on your study, the database can include

  • Participant screening and consent confirmation
  • Baseline characteristics
  • Exposure and risk-factor information
  • Clinical and behavioural outcomes
  • Repeated measurements
  • Scheduled follow-up forms
  • Participant status tracking
  • Loss-to-follow-up monitoring
  • Site and investigator access controls
  • Automated calculations and derived variables
  • Recruitment and completion dashboards
  • Export-ready structured datasets
Patient registries

Secure, structured registries for long-term data collection.

Registries can be configured for one or more conditions, sites, treatment pathways or patient groups, with user roles and permissions set according to each organisation's responsibilities.

The registry can grow with you, with new forms or follow-up stages added through a documented change-control process.

Registry functionality can include

  • Initial patient registration
  • Unique participant identifiers
  • Demographic and clinical information
  • Diagnosis and disease-history records
  • Treatment and medication information
  • Repeated clinical assessments
  • Patient-reported outcomes
  • Long-term follow-up
  • Site-specific access
  • Data-quality checks
  • Registry dashboards
  • Structured data export
Post-market studies

Capture real-world information on product performance, safety, usability and outcomes.

We support post-market surveillance studies for medical devices, healthcare products, digital-health technologies and other regulated or evidence-led products.

Data-capture workflows can cover

  • Participant and site registration
  • Product-use information
  • Device or product identification
  • Usage frequency and duration
  • Product-performance assessments
  • Safety events and complaints
  • User-experience feedback
  • Follow-up assessments
  • Conditional event notifications
  • Corrective-action follow-up
  • Trend monitoring
  • Study-specific reports
Actual-use and behavioural studies

Measure how participants use products, follow instructions and behave in real-world conditions.

We support studies that need repeated data collection, participant segmentation and detailed analysis of actions, experiences and outcomes.

A study can include

  • Participant eligibility and screening
  • Baseline attitudes and behaviours
  • Product-use instructions
  • Daily or scheduled activity records
  • Usage frequency and duration
  • Behavioural outcomes
  • Comprehension assessments
  • Product-handling questions
  • Participant feedback
  • Multimedia instructions
  • Follow-up assessments
  • Conditional questions and calculations
eDiary and ePRO data collection

Collect information directly from participants with electronic diaries and electronic Patient-Reported Outcome forms.

Participants complete questionnaires on a computer, tablet or mobile device, so outcomes and experiences are recorded closer to the time they happen.

Questionnaires are structured to avoid unnecessary questions and keep the participant experience as simple as possible.

A participant completes an electronic questionnaire on their phone at home

We can configure

  • Daily, weekly or event-based diaries
  • Symptom and severity scales
  • Quality-of-life assessments
  • Treatment-experience questionnaires
  • Medication-use records
  • Product-use diaries
  • Pain and discomfort scales
  • Participant-reported adverse events
  • Follow-up assessments
  • Completion monitoring
  • Conditional questions
  • Automated scores and calculations
  • Notifications based on defined responses
Consumer and market research

Reach participants in different countries and languages through one centrally managed data-capture system.

We configure multilingual questionnaires while keeping variable names, response codes and data outputs consistent across every language version.

Read more about multilingual data collection.

Projects can include

  • Consumer-use studies
  • Product evaluations
  • Concept testing
  • Customer-experience research
  • Healthcare market research
  • Brand and message testing
  • International surveys
  • Recruitment quotas
  • Participant segmentation
  • Randomised content
  • Image and video questions
  • Country-specific routing
  • Real-time reporting
  • Combined multilingual datasets