Pharmaceutical manufacturing facilities

Nick Taylor made this Rhyddid Gwybodaeth request to Medicines and Healthcare Products Regulatory Agency

This request has been closed to new correspondence from the public body. Contact us if you think it ought be re-opened.

Roedd y cais yn rhannol lwyddiannus.

Dear Sir or Madam,

I would like to make a request under the Freedom of Information Act(FOI).

Could you provide me with a list of registered GMP pharmaceutical production facilities in the UK?

I would like details of the address, company using the facility and first year of registration.

Thanks for your help

Yours faithfully,

Nick Taylor

MHRA Information Centre, Medicines and Healthcare Products Regulatory Agency

Dear Enquirer,

Thank you for your enquiry to the Information Centre at the MHRA.

Please accept this automated response as acknowledgement that your
enquiry has been received and will be dealt with as quickly as
possible.

Your enquiry will be dealt with as follows; straightforward requests
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Central Enquiry Point
Information Centre
Medicines and Healthcare products Regulatory Agency

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References

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MHRA Information Centre, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 10/182

Dear Mr Taylor,

RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000

Thank you for your enquiry which we received on 8th April 2010.


I confirm that your request is 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.

Yours Sincerely

Central Enquiry Point
Information Centre
MHRA
Market Towers
London SW8 5NQ

Tel: +44 (0)207084 2000
FAX: +44 (0)207084 2353

dangos adrannau a ddyfynnir

Jackson, William, Medicines and Healthcare Products Regulatory Agency

1 Atodiad

  • Attachment

    Department of Health and MHRA Register of Licensed Manufacturing Sites Human Veterinary and Combined Sites 2010 April 2010 1.pdf

    1.1M Download View as HTML

6th May 2010

Dear Mr Taylor,

REF: 10/182

Please find attached the information that you requested under the Freedom
of Information Act.

<<Department of Health and MHRA Register of Licensed Manufacturing Sites
(Human Veterinary and Combined Sites) 2010 - April 2010[1].pdf>>

Please note we are unable to provide the first year of registration.
Section 12 of FOIA provides that public authorities are not required to
comply with requests that they judge to constitute an excessive use of
their resources. Your request asked for the first year of registration and
we therefore consider that the section 12 provision applies in this
instance.

As this information on the first year of registration is not readily
available it would be necessary to locate and consider a large number
reports to compile such a comprehensive list. The resource required to
complete this work will exceed the relevant limit in the FOIA of £600,
calculated at £25 per hour and would in fact be in excess of 24hours. I
do not consider, in this case, that there is an overriding public interest
in undertaking this work.

If you have a query about this letter, please do not hesitate to contact
me at [email address]

If you are unhappy with our decision, you may ask for it to be reviewed.
That review will be undertaken by a senior member of the Agency who has
not previously been involved in your request. If you wish to peruse that
option please write to the Communications Directorate, 10th Floor,
Medicines and Healthcare products Regulatory Agency, at the above address
quoting the above reference.

After that, if you remain dissatisfied, you may write to the Information
Commissioner at;

The Information Commissioner's Office

Wycliffe House

Water Lane

Wilmslow

Cheshire

SK9 5AF

They will make a decision on whether or not we have interpreted the FOIA
correctly in withholding information from you.

Yours sincerely

Will Jackson

MHRA

Inspection and Standards

cc R Goldfinch
S Wilson

Copyright notice

The information supplied in response to your request is the copyright of
MHRA and/or a third party or parties, and has been supplied for your
personal use only. You may not sell, resell or otherwise use any
information provided without prior agreement from the copyright holder.
For full details on our copyright policy please visit:

[1]http://www.mhra.gov.uk/home/Idcplg?IdcSe...
or e-mail the [2]MHRA Information Centre

This email and any files transmitted with it are confidential. If you are
not the intended recipient, any reading, printing, storage, disclosure,
copying or any other action taken in respect of this email is prohibited
and may be unlawful.

If you are not the intended recipient, please notify the sender
immediately by using the reply function and then permanently delete what
you have received.Incoming and outgoing email messages are routinely
monitored for compliance with the Department of Healths policy on the use
of electronic communications.

For more information on the Department of Healths email policy, click

http://www.dh.gov.uk/DHTermsAndCondition...

dangos adrannau a ddyfynnir

Communications via the GSi may be automatically logged, monitored and/or
recorded for legal purposes.

References

Visible links
1. http://www.mhra.gov.uk/home/Idcplg?IdcSe...
2. mailto:[MHRA request email]

Dear Mr Jackson,

Thank you for your help with this matter.

Yours sincerely,

Nick Taylor