ANNEX IU.K.Requirements for accreditation, designation, authorisation or licensing of tissue establishments as referred to in Article 3

C.EQUIPMENT AND MATERIALSU.K.

1.All equipment and material must be designed and maintained to suit its intended purpose and must minimise any hazard to recipients and/or staff.U.K.

2.All critical equipment and technical devices must be identified and validated, regularly inspected and preventively maintained in accordance with the manufacturers' instructions. Where equipment or materials affect critical processing or storage parameters (e.g. temperature, pressure, particle counts, microbial contamination levels), they must be identified and must be the subject of appropriate monitoring, alerts, alarms and corrective action, as required, to detect malfunctions and defects and to ensure that the critical parameters are maintained within acceptable limits at all times. All equipment with a critical measuring function must be calibrated against a traceable standard if available.U.K.