Your Advice to MHRA on UK Government experimental Covid vaccine program

Mae'r ymateb i'r cais hwn yn hwyr iawn. Yn ôl y gyfraith, ym mhob amgylchiad, dylai Commission on Human Medicines fod wedi ymateb erbyn hyn. (manylion). Gallwch gwyno drwy yn gofyn am adolygiad mewnol.

Dear Commission on Human Medicines,

please provide all communications providing "advice" to the MHRA from you (CHM) relating to the UK Government experimental Covid vaccine program.

Kindly also provide the names and GMC number of the GMC registered Doctors who are responsible for providing such advice.

Please note the MHRA on a Letter dated 14 July 2021 to Brian Gerrish of UKcolumn.org and signed by Dr. Sarah Branch has confirmed CHM has provided such advice.

Yours faithfully,

Gian A. Ameri

MHRA Customer Services, Commission on Human Medicines

Thank you for your email.  This auto-response is to inform you that your
email has been received and will be reviewed by our Customer Service Team.
We will respond to you as soon as possible. 

 

Please note that we may not respond if your query: 

 

• contains offensive language
• has already been answered in a previous reply to you
• is illegible
• is selling or promoting a product
• is for information only 

 

Medicines and Healthcare products Regulatory Agency
10 South Colonnade, 
Canary Wharf, 
London 
E14 4PU
gov.uk/mhra
Stay connected 
 
For information on how the Agency uses your personal data and your data
protection rights, please see our three centres’ Privacy Notices: MHRA,
CPRD and NIBSC. 

 

The UK has left the EU, and the transition period ends on 31 December
2020. Our [1]guidance and information can be accessed here. 

References

Visible links
1. https://www.gov.uk/government/collection...

MHRA Customer Services, Commission on Human Medicines

Our Ref: FOI 21/830
       
Dear Gian A Ameri,
       
RE:  REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000
        
Thank you for your enquiry which we received on 20th July 2021.
  
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 Service Centre
 
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU
Telephone 0203 080 6000

dangos adrannau a ddyfynnir

MHRA Customer Services, Commission on Human Medicines

FOI 21/830

 

Dear Gian A. Ameri

 

Thank you for your email.

 

Unfortunately, the information you have requested is exempt under Section
12 (unreasonable use of resources) of the Freedom of Information (FOI)
Act. Section 12 of the Act allows public authorities to refuse requests
where the cost of dealing with them would exceed the appropriate limit,
which for central government is set at 24 working hours in determining
whether the department holds the information, locating, retrieving and
extracting the information. As your request concerns large amounts of
information, it will not be possible to complete this part of your request
within the 24 working hours stipulated in the FOI Act. For this reason, we
are not processing your request further.

 

CHM minutes and papers covering many vaccines and across several months is
available to view at the following link of our website page below.

[1]https://www.gov.uk/government/organisati...

 

Membership of CHM is available to view at this link.

[2]https://www.gov.uk/government/organisati...

 

We confirm that we do not give out GMC numbers.

 

If you disagree with how we have interpreted the Freedom of Information
Act 2000 with regards to your request, you can ask for the decision to be
reviewed. The review would be carried out by a senior member of the Agency
who was not involved with the original decision.

 

If you have a query about the information provided, please reply to this
email.

 

 

Yours sincerely

 

 

MHRA Customer Service Centre

 

Medicines and Healthcare products Regulatory Agency

10 South Colonnade, Canary Wharf, London E14 4PU

 

 

dangos adrannau a ddyfynnir

Dear MHRA Customer Services,

this is a formal request for an Appeal to your decision and a further internal review.

Surely all the data you hold and which I have requested you hold in electronic format and therefore the cost limit you quote is not applicable to this FOI request.

Therefore, kindly produce all data you hold in electronic format to include the names and GMC number, if applicable, of those responsible for the data.

Yours sincerely,

Gian A. Ameri

MHRA Customer Services, Commission on Human Medicines

Thank you for your email.  This auto-response is to inform you that your
email has been received and will be reviewed by our Customer Service Team.
We will respond to you as soon as possible. 

 

Please note that we may not respond if your query: 

 

• contains offensive language
• has already been answered in a previous reply to you
• is illegible
• is selling or promoting a product
• is for information only 

 

Medicines and Healthcare products Regulatory Agency
10 South Colonnade, 
Canary Wharf, 
London 
E14 4PU
gov.uk/mhra
Stay connected 
 
For information on how the Agency uses your personal data and your data
protection rights, please see our three centres’ Privacy Notices: MHRA,
CPRD and NIBSC. 

 

The UK has left the EU, and the transition period ends on 31 December
2020. Our [1]guidance and information can be accessed here. 

References

Visible links
1. https://www.gov.uk/government/collection...

MHRA Customer Services, Commission on Human Medicines

Internal Review of FOI 21/830
 
Dear Gian A. Ameri,
 
Thank you for your email.
 
We confirm that an internal review will be carried out on FOI 21/830. We normally aim to respond to requests for internal review within 20 working days of receipt. However, due to high volumes of queries we are currently receiving related to COVID-19 please be aware that responses may take longer than usual.
 
Kind Regards
 
 
MHRA Customer Service Centre
 
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU

dangos adrannau a ddyfynnir

Dear MHRA Customer Services,

you failed to respond to my FOI request in a timely manner.

By law, you should normally have responded promptly and by 18 August 2021.

Please respond.

Yours sincerely,

Gian A. Ameri

MHRA Customer Services, Commission on Human Medicines

Thank you for your email.  This auto-response is to inform you that your
email has been received and will be reviewed by our Customer Service Team.
We will respond to you as soon as possible. 

 

Please note that we may not respond if your query: 

 

• contains offensive language
• has already been answered in a previous reply to you
• is illegible
• is selling or promoting a product
• is for information only 

 

Medicines and Healthcare products Regulatory Agency
10 South Colonnade, 
Canary Wharf, 
London 
E14 4PU
gov.uk/mhra
Stay connected 
 
For information on how the Agency uses your personal data and your data
protection rights, please see our three centres’ Privacy Notices: MHRA,
CPRD and NIBSC. 

 

The UK has left the EU, and the transition period ends on 31 December
2020. Our [1]guidance and information can be accessed here. 

References

Visible links
1. https://www.gov.uk/government/collection...

MHRA Customer Services, Commission on Human Medicines

1 Atodiad

  • Attachment

    FOI 21 830 CSC 62643 Internal review of Freedom of Information request Your Advice to MHRA on UK Government experimental Covid vaccine program.txt

    5K Download View as HTML

Dear Gian A. Ameri,

Thank you for your email.

We replied to your request (our reference FOI 21/830) on 11 August 2021. We received your reply, in which you requested an internal review, on 11 August 2021. We responded on 12 August 2021 to confirm that we would conduct an internal review (please find attached a copy of that email for your convenience).

As noted in the attached email, we normally aim to respond to requests for internal review within 20 working days of receipt. However, due to high volumes of queries we are currently receiving related to COVID-19 please be aware that responses may take longer than usual.

Kind Regards

MHRA Customer Service Centre
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU

dangos adrannau a ddyfynnir