Statistical support during the trial

Description of service

After the clinical trial(s) has been designed, we can assist you through trial set-up and continue to provide statistical support whilst the trial is ongoing.

Services we offer include:

• Authoring the statistical sections of the protocol and full review of the protocol to ensure consistency and that data collection are appropriate
• Authoring the statistical analysis plan (SAP)
• Review of case report forms (CRFs)
• Review of data management documentation
• Assist with submissions to health authorities, either for advice or SPA process
• Provide statistical attendance to study investigator meetings
• Provide statistical analysis and a comprehensive statistical report
• Review of tables, figures and listings
• Statistical QC
• Statistical training for your staff

Why choose us?

• We understand the peaks and troughs within drug development and also that speed is of the essence. We can provide the flexible support you need
• We can provide guidance to your in-house statistician or work as the responsible statistician on your study team, alongside other medical professionals