Freedom of Information request an investigation “into the matter of Mr Bourne receiving/awarded £30 Million in order to supply test tubes and whether it includes the former Secretary of State for Health Mr Matt Hancock. (FOI 21/1181)
Published 26 May 2022
© Crown copyright 2022
This publication is licensed under the terms of the Open Government Licence v3.0 except where otherwise stated. To view this licence, visit nationalarchives.gov.uk/doc/open-government-licence/version/3 or write to the Information Policy Team, The National Archives, Kew, London TW9 4DU, or email: [email protected].
Where we have identified any third party copyright information you will need to obtain permission from the copyright holders concerned.
This publication is available at https://www.gov.uk/government/publications/freedom-of-information-responses-from-the-mhra-week-commencing-29-november-2021/freedom-of-information-request-an-investigation-into-the-matter-of-mr-bourne-receivingawarded-30-million-in-order-to-supply-test-tubes-and-whether
FOI 21/1181
29th November 2021
Dear,
Thank you for your email dated 1st of November where you asked about an investigation “into the matter of Mr Bourne receiving/awarded £30 Million in order to supply test tubes. Is your investigation ongoing ,if so ,does it include the former Secretary of State for Health Mr Matt Hancock.”
We are pleased to provide you with the following information.
MHRA responded swiftly to the allegations concerning Hinpack and focused on their medical device production activities in line with the Medical Device Regulations 2002 as amended. Appropriate steps were taken to ensure patient safety is maintained and our enquiry has been concluded. The MHRA are unable to provide updates as to the state of any referrals or investigations. This is in accordance with section 237 of the Enterprise Act 2002 (“the Act”). Section 237 of the Act, read with schedule 14 thereof, restricts the disclosure of information about the affairs of an individual or any business if that information comes to the MHRA in connection with the exercise of any function it has under or by virtue of the Devices Regulations.
The UK Medical Device Regulations does not extend to purchasing contracts. The MHRA continues to monitor the marketing and supply of devices on the UK market and takes action where a device compromises patient safety.
If you have a query about this, please reply to this email.
If you are dissatisfied with the handling of your request, you have the right to ask for an internal review. Internal review requests should be submitted within two months of the date you receive this response and addressed to: [email protected] Due to the ongoing Covid-19 situation, we are not able to accept delivery of any documents or correspondence by post or courier to any of our offices. Please remember to quote the reference number above in any future communications.
If you were to remain dissatisfied with the outcome of the internal review, you would have the right to apply directly to the Information Commissioner for a decision. Please bear in mind that the Information Commissioner will not normally review our handling of your request unless you have first contacted us to conduct an internal review. The Information Commissioner can be contacted at:
Information Commissioner’s Office
Wycliffe House
Water Lane
Wilmslow
Cheshire
SK9 5AF
Yours sincerely
Enquiries Co-ordinator
Devices Division