Dear Medicines and Healthcare Products Regulatory Agency,

Please can I have a copy of all of the post inspection letters for Testerworld Limited for the period of 12 month prior to their licence suspension in March 2021.

Yours faithfully,

John Watts

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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________________________________________ From: John Watts
<[FOI #861297 email]> Sent: Thursday, May 12, 2022
6:57:09 AM To: MHRA Customer Services Subject: Freedom of Information
request - Testerworld Limited Dear Medicines and Healthcare Products
Regulatory Agency, Please can I have a copy of all of the post inspection
letters for Testerworld Limited for the period of 12 month prior to their
licence suspension in March 2021. Yours faithfully, John Watts
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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 22/698

Dear John Watts,

RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000

Thank you for your enquiry which we received on 12th May 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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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

FOI 22/698

Dear Mr Watts,

Thank you for your information request, dated 12 May 2022, where you asked for:

"Please can I have a copy of all of the post inspection letters for Testerworld Limited for the period of 12 month prior to their licence suspension in March 2021"

Unfortunately, the information is exempt from release under section 30:

Section 30 - Investigations: the information you have requested concerns an active Agency investigation and it is therefore exempt under section 30 of the FOI Act, which concerns investigations and proceedings conducted by public authorities. Section 30 is a qualified exemption, which means that we have considered whether the public interest in releasing the information is outweighed by the public interest in not giving the information.

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: [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 Customer Experience Centre

Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU Telephone 0203 080 6000

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