Question about FOI refs. 21/957 and 22/554

Waiting for an internal review by Medicines and Healthcare Products Regulatory Agency of their handling of this request.

Dear Medicines and Healthcare Products Regulatory Agency,

Are the two vials of COVID-19 vaccine referenced in MHRA FOI 21/957 of the same two lot numbers mentioned in MHRA FOI 22/554?

A one-word answer is acceptable.

Yours faithfully,

Matt Cooper

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 22/1147

Dear Matt Cooper,

RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000

Thank you for your enquiry which we received on 16th November 2022.

I confirm that your request is now being handled under the Freedom of Information Act and you should receive a reply within 20 working days from our date of receipt.

If you need to contact us again about this request, please quote the reference number above.

Please be aware that we publish FOIs replies and these are redacted and are located on our website at the following link below.
https://www.gov.uk/government/collection...

Kind Regards,

MHRA Customer Experience Centre
Communications and engagement team
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU Telephone 020 3080 6000

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Dear MHRA Customer Services,

I await your response to this request.

Yours sincerely,

Matt Cooper

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Dear Matt Cooper,

 

Thank you for your request; please accept our apologies for the delay in
sending this response.

 

Your request: Are the two vials of COVID-19 vaccine referenced in MHRA FOI
21/957 of the same two lot numbers mentioned in MHRA FOI 22/554?

A one-word answer is acceptable.

 

Our response: We believe the reference in your query should have been FOI
21/997 rather than 21/957. We have therefore based our review on that
reference.

In FOI 22/554 we indicated that vials tested from two batches of COVID-19
vaccine did not meet the required specification for one test: these
batches were not certificated by MHRA/NIBSC.

FOI 21/997 refers to vaccine lots there were not distributed to the UK and
were not tested by MHRA.

There is therefore no overlap.

 

If you have a query about the information provided, 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: [1][MHRA request email]

 

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,

 

MHRA FOI Team

 

 

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Dear Medicines and Healthcare Products Regulatory Agency,

Please pass this on to the person who conducts Freedom of Information reviews.

I am writing to request an internal review of Medicines and Healthcare Products Regulatory Agency's handling of my FOI request 'Question about FOI refs. 21/957 and 22/554'.

I apologise if my request was unclear, so I will provide a link to the response provided by yourselves on 8 December 2021, which states a reference of 21/957:

https://www.whatdotheyknow.com/request/c...

A full history of my FOI request and all correspondence is available on the Internet at this address: https://www.whatdotheyknow.com/request/q...

Yours faithfully,

Matt Cooper

Dear MHRA Customer Services,

I await your response to my request for an internal review.

Yours sincerely,

Matt Cooper

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Dear Matt Cooper,

 

Thank you for your email.

 

We acknowledge that the Internal Review request is outstanding and we
apologise for the delay.

 

The review is currently being conducted and we hope to respond to you as
soon as we can.

 

Kind Regards

 

 

MHRA Customer Experience Centre

Communications and engagement team

Medicines and Healthcare products Regulatory Agency

10 South Colonnade, Canary Wharf, London E14 4PU

 

 

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CHP Gillow left an annotation ()

This FOIR was raised on 16 November 2022 and recorded on the MHRA's internal system as having been responded to on 19 December. The text field for the respo9nse is blank in the MHRA database.

Significantly, despite the author's request for an Internal Review, there is no record of an IR having been initiated by the MHRA.

CHP Gillow left an annotation ()

Apologies: the request for an internal review was made on 8 August AFTER the end date of the data I hold...