MHRA Register of Licensed Wholesale Distribution Sites
Dear Medicines and Healthcare products Regulatory Agency,
Please provide a spreadsheet for all WDA(H) licensed sites including the following information under each column:
- Licence Holder Company Name
- Licence Holder Trading Name
- Licence Holder Address
- Licence Holder Contact Name
- Licence Holder Contact Email
- Licence Holder Contact Phone Number
- Licence Holder Responsible Person (If different from contact name)
- Responsible Person Email
- Responsible Person Phone Number
- Site Address
- Site ID
- Scope of WDA
Yours faithfully,
Mrs Wingrove
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Clinical trials of medicines and Clinical investigation for a medical
device:
[1]https://www.gov.uk/medicines-medical-dev...
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[2]https://www.gov.uk/apply-for-manufacture...
Registration of medical devices, opticians and dental laboratories:
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[4]https://www.gov.uk/report-problem-medici...
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Kind regards
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Communications division
Medicines and Healthcare products Regulatory Agency
151 Buckingham Palace Road, London, SW1W 9SZ
Telephone: 020 3080 6000
Email: [8][MHRA request email]
Please note this is an automated reply; please do not respond to this
message.
Our Ref: FOI 15/570
Dear Mrs Wingrove,
RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000
Thank you for your enquiry which we received on 12 November 2015.
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.
Kind Regards,
Customer Services
Communications division
Medicines and Healthcare Products Regulatory Agency
151 Buckingham Palace Road, London, SW1W 9SZ
Telephone: 020 3080 6000
Email: [MHRA request email]
Stay connected: mhra.gov.uk/stayconnected
19/11/2015
Mrs Wingrove
[1][FOI #302075 email]
Dear Mrs Wingrove
REF: FOI 15/570
Thank you for your communication to the MHRA in relation to a Freedom of
Information request for a spreadsheet containing all WDA(H) licensed
sites.
The following information is exempt under Section 21 of the Freedom of
Information Act (FOIA), because the information is accessible to you, as
it is already in the public domain: Licence Holder company name, licence
holder trading name, licence holder address, site address, site id, scope
of WDA. Information on WDA(H) licenced sites can be located on EudraGMP.
EudraGMP is a public access website. The website address for EudraGMP is
as follows: [2]http://eudragmp.eudra.org
Information relating to personal data such as licence holder contact name,
telephone number, email etc. is exempt under Section 40 of the Freedom of
Information Act (FOIA) because the information requested contains elements
of personal data, the disclosure of which would be unfair in that it would
breach the first principle of the Data Protection Act which says that
information must be processed fairly and lawfully.
If you have a query about this letter, please do not hesitate to contact
me at [3]IE&[email address]
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 of receipt of the response to your
original letter and should be addressed to: Communications Directorate,
Medicines and Healthcare products Regulatory Agency, 151 Buckingham Palace
Road, London, SW1W 9SZ. Please remember to quote the reference number
above in any future communications.
After that, if you remain dissatisfied, you may write to the Information
Commissioner at;
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 handling your request.
Yours sincerely,
Grace Perry
MHRA
Inspection, Enforcement and Standards
cc Policy Manager
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