Clinical Research - Use of Electronic Signatures

The purpose is to outline the procedure for the use of electronic signatures on records for clinical research, in compliance with NSW Health, SCHN and regulatory requirements. Adherence to this procedure will ensure: * Quality control systems and procedures are enacted to ensure the appropriate use of electronic signatures; * Improved consistency and efficiencies in workflow processes for clinical research personnel; and * Appropriate records detailing the chain of custody for original documents involving electronic signatures are maintained at all times;