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…
24.3: General requirements 24.3.1: Label quality Labels used for tissue and sample labelling must be: self-adhesive using a non-invasive adhesive
24.2: The labelling system The labelling system for retrieved tissues and tissue products comprises the following elements: Base label: The l…
23.4: Donation identification numbers (DIN) 23.4.1: General structure The donation identification number (‘donation number’) – ICCBBA Data Structure 001, plays a cr…
23.2: The labelling system The labelling system for blood and blood components comprises the following elements: The base label: The label ap…
1.3: Other institutions involved in developing guidelines and regulations relevant to the UK A brief description of some international organisations and their interrelationships is requir…
1.2: Organisation of the UK Blood Services There are four national Blood Services/Blood Transfusion Services in the UK: NHS Blood and Transplant (NHSBT), a Special Health …
26.2: Specification The layout of the blood pack base label is shown in Figure 26.1 and is divided into three areas. Area numbers on the diagram are for reference purposes only and must n…
24.1: Introduction The ISBT 128 Standard is an internationally defined coding system for the barcoding of information on blood components, progenitor cells and tissues. Designed by the In…
23.6: Component labels 23.6.1: General description These labels are for use on blood collection packs and/or satellite packs. Each label will display a component description pri…
23.1: Introduction 23.1.1: General information The information contained in this chapter is intended to inform all persons involved in labelling blood and blood components of th…
1.4: References 1. Statutory Instrument 2005 No. 50. The Blood Safety and Quality Regulations 2005. Available at www.legislation.gov.u…
1.1: Development of the Red Book Guidelines for the Blood Transfusion Services in the United Kingdom was first published in 1990 by HMSO. It was compiled by experts …
rtc-lo_2012_05_pres_moss.pdf (199KB)
rtc-sw_2013_08_R_yuen.pdf (411KB)
rtc-sw_2013_08_R_allford.pdf (508KB)
rtc-lo_2012_05_pres_wilson.pdf (563KB)