Clinical Risk Management Plan - One of the three documents that manufacturers and healthcare organisations are required to create when they design and implement health IT systems. The document (often simply called the 'Plan') sets out the activities which a manufacturer or healthcare organisation intends to undertake in order to assure the system and proactively manage any clinical risk.
Safehand provides expert consultancy services to manage clinical risk in health IT systems, maintain patient safety and comply with standards DCB 0129 and DCB 0160. www.safehand.co.uk.