SUPPORT

Below is a list of the typical areas we can offer assistance:
Complete a study specific auditPreparing for auditPreparing your study for GCP inspectionInterview preparation for audit/inspectionStudy set upAdvice in writing protocols and patient information sheetsFinding out the country specific regulatory issuesSubmission documentation for CTIMP's and EthicsCompleting the IRAS formStudy close downShort term monitoringWriting standard operating procedures

Please note there are numerous sites which have been specifically developed to assist clinical researchers in the above areas. We encourage you to make use of this free information and resources before contacting us.

For example, are you new to completing the IRAS form? The IRAS site has a free e learning module to guide you step by step through completing the form.

Our links page will have some of these sites