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
