EDC Trial Management

EDC Trial Management

EDC technology – flexible to meet your trial needs

SQN Health EDC provides an innovative and effective clinical, data management and reporting environment that has been extensively used by global pharma, biotech and other CRO companies to support the simplest and most complex international trial designs.

It combines ease of data collection with extensive project management and clinical oversight and consistently delivers high quality data while minimising the risks commonly associated with this process. There will never be the need to compromise your study design because of functional limitations found in other EDC systems.

Intuitive EDC system and processes

Everything about our EDC system is designed to help you run successful trials, mitigating risk and shortening your time to market. Site staff and monitors love it!

The ease of initial set-up means your trial can get underway quickly; six to ten weeks from final protocol is common. This is facilitated by advanced technology using an extensive library of study design and eCRF elements. This library approach is CDISC-based and can incorporate your company and study-specific eCRF components allowing efficient and cost-saving use within and across multiple trials.

If you require native local language support, no problem, this can be provided with ease.

SQN Health EDC v4 – Coming Soon

Our EDC system, Syne-clin will ease the management of your study, including

  • Reducing risk with real time access to customisable reports
  • Integrated query management and oversight
  • Integration of ePRO, Diary Cards, IxRS, Laboratory data, Images etc
  • Oversight of protocol violators
  • Support to SAE expedited reporting and PV integration
  • Use of mobile devices, including tablets and smartphones
  • Support to DSMBs (including Patient Profile reports)
  • Real-time data extraction for further review and analysis
  • Fully integrated statistical analysis and reporting
  • Providing a data package that confidently meets regulatory requirements
  • 24/7/365 interactive helpdesk with local language support where required

Personalised and web-based training ensures smooth initiation of trials and includes assessment of user competence and certification.  The need for helpdesk support is substantially reduced, aiding continuity of data collection processes and supporting high user satisfaction across the clinical team.

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