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    WMS » Warwick Clinical Trials Unit

    • About us
    • News & events
    • Trials in Progress
    • Conducting a Clinical Trial
      • Initial Planning
      • Set up
      • During the Trial
      • After the Trial
    • Trials methodology
    • Publications
    • Contact us
    • Intranet
    • Disclaimer
    University of Warwick

    Conducting a Clinical Trial

    These pages provide advice about the running of a clinical trial, from inception to publication.

    WMS staff have access to the complete set of

    Standard Operating Procedures for all aspects of running a clinical trial.

    WMS staff should also refer to the University of Warwick Ethics and Research Governance policy.

    Please refer to the Collaborating with WCTU page to find information on services WCTU can provide to assist in running a trial.


    Initial PlanningSet upDuring the TrialAfter the Trial


    A Criminal Records Bureau (CRB) check may be required for staff working on trials, for more information and to see if your role requires a CRB check, please refer to this document.



    The University has a responsibility and is committed to ensuring that the research conducted by its staff and students maintains the highest possible standards of integrity. The Research Code of Conduct provides guidelines on the standards of work performance and ethical conduct expected of all persons engaged in research at the University.

    Failure to comply with the research code may constitute research misconduct. A Code of Practice for the Investigation of Research Misconduct has recently been approved by the University Senate and Council and should be followed for any allegations of potential misconduct.


     

     

    Key people

    Claire Daffern Quality Assurance Manager

    Dr Sarah Duggan Clinical Trials Unit Manager


    Links

    Links to Legislation
    MRC Clinical Trials Toolkit
    National Research Ethics Service (NRES)
    Integrated Research Application System (IRAS)
    Medicines and Healthcare products Regulatory Authority (MHRA)
    NHS R&D Forum
    Research Support ServicesNRES Toolkit: Adults lacking capacity to consent to researchMHRA site for Physiotherapists and Occupational Therapists
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    Staff IntranetCurrent Students
    Warwick Medical School
    The University of Warwick
    Coventry
    CV4 7AL
    Tel: +44 (0) 2476 574 880
     
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    Page contact: Claire Daffern Last revised: Mon 14 Nov 2011
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