Standard Operating Procedures
The suite of KHP CTO Clinical Trial SOPs are developed and rolled out across the Partner Organisations by the Clinical Trials Training Executives
as each SOP is approved. The list of SOPs required is a living document and the SOPs are at different stages of development. Training will be
developed and delivered as SOP's are brought into effect.
All SOPs are controlled documents. The guidance document (below) on version controlling documents, is applicable to all documents
produced by the KHP CTO, including but not limited to SOPs, Template documents and Training Presentations. It may also apply to documents
produced by Investigator sites, including but not limited to Clinical Trial Protocols, Patient Information Sheets (PIS) and Consent
forms and Case Record Forms.
Version Control Guidelines (22Kb)
Related Information
www.mhra.gov.uk
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