Full CDM handover information should be provided. Every test and inspection should be recorded and retained under local governance agreed with the Group; manufacturers should certify plant and devices to current standards; fixed wiring records follow BS 7671 forms. Records should include test certificates (electrical and pressure), declarations of conformity, design standards and dates, design departures, design data and cable calculations, installation certificates, supplementary bonding certificates for Group 1 and 2 locations, prefabricated wiring test standards, Medical Location drawings and changes of use, earthing drawings, mains and earthing schematics, O&M manuals and maintenance schedules, site-specific specifications, pre-handover fault logs and details of Medical IT, UPS, generators and panels.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.