HSE banner

GE Healthcare Ltd, Maynard Centre Site, Cardiff

Quarterly Report for 1 July to 30 September 2007

Contents


Foreword

This report is issued as part of the Health and Safety Executive's commitment to make information about inspection and regulatory activities relating to the above site available to the public. It is for distribution to members of the GE Healthcare Ltd Maynard Centre Local Liaison Committee (LLC) and covers activities associated with the regulation of safety at the site. These reports are distributed quarterly and are available also from the Internet at www.hse.gov.uk/nuclear/llc/index.htm. Site Inspectors of HM Nuclear Installations Inspectorate attend LLC meetings and will be happy to respond to any questions raised there by members. Any other person wishing to enquire about matters covered by this report may contact HSE’s Nuclear Directorate Information Centre on 0151-951-4103.

Nuclear Safety Directorate
Health and Safety Executive
Redgrave Court
Merton Road
Bootle
Merseyside
L20 7HS


Inspections

NII inspections were made on 21–22 August 2007. (Inspections are also made at GE Healthcare Ltd’s nuclear licensed sites at Amersham (the Grove Centre) and Harwell. Where these are relevant to the Maynard Centre they are included below. For instance, the sites have many arrangements in common for compliance with the conditions attached to their site licences.)


[back to top]

Routine matters

Inspections are undertaken for the purpose of monitoring compliance with (i) the conditions attached by HSE to the nuclear site licences, and (ii) other relevant provisions of the Health and Safety at Work etc Act 1974, including the Ionising Radiations Regulations 1999. In this period routine inspections included:

  1. The production, storage, and recording of waste, and its preparation for disposal.
  2. Arrangements for the notification, recording, investigation, and reporting of incidents on the site.

Issues arising from these and previous inspections are being pursued.


[back to top]

Non-routine matters

Corporate

Modifications: As required by NII, GE Healthcare Ltd has submitted new draft arrangements for the control of modifications to the plant and processes. These drafts have been discussed at meetings between the two parties, and form the first phase of an improvement programme for these and associated arrangements.

Maynard Centre

Waste: The Environment Agency and NII made a joint inspection of waste facilities and waste records.

Ventilation: An inspection of the air-handling areas saw evidence of extensive refurbishments, but found deficiencies in provision of fire exit signs, which were corrected promptly by the licensee.

No statutorily reportable incidents were notified to NII in this quarter.


[back to top]

Regulatory activity

As part of its regulation under the nuclear site licence NII issues formal regulatory documents, which include Consents, Approvals, Directions, and Licence Instruments1. No such documents were issued in this quarter.

No other issues have arisen that have required formal regulatory action.


[back to top]

1 Licence Instruments are issued: to acknowledge receipt of specified documents, eg proposals for a new or modified plant; to stipulate whether the Inspectorate intends to examine these documents; or to agree to the start of a particular phase of construction, commissioning, modification, or decommissioning.