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.
All SOP documents are available as .pdf documents. If you do not have a .pdf reader installed, please follow the link below to download Adobe Reader.