DATA MANAGEMENT

Your trial is unique to your needs

Your trial is unique, therefore it is paramount your data management support is flexible to suit your needs – the way your data are collected and managed will impact on the overall quality and efficiency of your trial.

Our world-class data management team and EDC/ePRO technology, supported by effective quality management processes are used to ensure your data are reliable, compliant, secure and delivered on time.

Fully customisable data management services

With an emphasis on quality standards, our team will ensure your study is completed within the shortest possible timeframe, creating a cost-effective solution that refuses to compromise on excellence.

With our help you are assured of:

  • Effective patient safety management
  • Tailored design of your eCRF/CRF/ePRO and clinical database
  • Innovative patient-centric data collection technology
  • Full risk management of your data
  • Real-time access to all your data at any time
  • Processes and data quality that meet QA and regulatory guidelines in every respect

Quality built in

Our team will ensure your study is completed within the shortest possible timeframe, creating a cost-effective solution that refuses to compromise on quality.

Client-specific libraries facilitate rapid database set-up and study initiation as well as accelerated analysis and reporting. CDISC-based processes (CDASH, SDTM, ADaM and define.xml) support the delivery of high quality data.

It just works

By choosing SQN’s fully integrated trial management and data management services, trial oversight is greatly enhanced. Easy access to data is available 24/7, providing you with powerful, flexible and real-time reporting of project management and clinical metrics through interactive, personalised dashboards and access to patient data.

SQN EDC Trial Management with Advanced Data Visualisation

SQN 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.

Studies using our software are deployed natively with a standard suite of dashboard reports providing real-time project management and clinical oversight information. Graphical presentation provides summary level views with single-click drilldown to the underlying study and subject records. Such functionality can be invaluable for safety assessments and more.


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