rtc-wmids_bedside_audit_survey_tool.doc (65KB)
rtc-sec_mins_rtc_conf_12_04_18.pdf (94KB)
rtc-em_bbt3_action_plan.doc (88KB)
Proforma (2006) used to collect data for this audit on the management of patients found to be anaemic during an emergency admission to hospital. For further details contact
rtc-scent_anaemia_proforma.pdf (8KB)
rtc-scent_audit_major_haemorrhage.pdf (14KB)
rtc-nw_ffp_audit_pres.pdf (167KB)
27.4: References 1. Council Directive 93/42/EEC of 14 June 1993 concerning medical devices. OJ, L 169, 12.7.1993, pp1–43. 2. Refere…
27.2: Specification All critical consumables used in the manufacture of therapeutic product that either come into contact with the therapeutic or influence its quality or the safety of re…
27.1: Introduction This chapter defines the requirements of the UK Blood Transfusion Services for the labelling by the manufacturer of ‘stand-alone’ consumable medical devices (critical c…
25.3: General protocol The general protocol defines the general character of the overall message, and elements which are common to both the envelope and the message content. The mes…