Trial management

Our trial management team can support you in the effective delivery of your trial, ensuring optimal recruitment and conduct of the study by providing:

• Registration of the study on the appropriate publically accessible database
• Co-ordination of Integrated Research Application System (IRAS) submission to obtain the appropriate approvals i.e. Research Ethics Committee (REC), Health Research Authority (HRA) and Medicines and Healthcare products Regulatory Agency (MHRA)
• Site selection, set up and ongoing management 
• Monitoring of the trial to ensure conduct according to protocol and key legislation
• Oversight and escalation of safety reporting for the trial
• Maintenance of study documentation and filing
• A central point of contact for queries and general facilitation of the trial
• Support for the reporting requirements of the trial, i.e. preparation of Annual Progress Reports to REC and HRA
• Close out of the trial, and preparation for archiving  
   

Please get in touch with us as soon as you have a research idea so as to get the appropriate support.