FOI release

Freedom of Information responses from the MHRA - week commencing 1 February 2021

Medicines and Healthcare products Regulatory Agency (MHRA) responses to freedom of information (FOI) requests for week commencing 1 February 2021

Documents

GDP Inspection Report 1 (FOI-21-003)

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GDP Inspection Report 2 (FOI-21-003)

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Annex 4 - Specific adverse drug reaction follow up forms (FOI-21-011)

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Lacosamide Additional Information (FOI-21-011)

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Pharmacovigilance inspection reports 1 (FOI-21-16)

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Pharmacovigilance inspection reports 2 (FOI-21-16)

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If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email [email protected]. Please tell us what format you need. It will help us if you say what assistive technology you use.

Pharmacovigilance inspection reports 3 (FOI-21-16)

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Pharmacovigilance inspection reports 4 (FOI-21-16)

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Pharmacovigilance inspection reports 5 (FOI-21-16)

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Pharmacovigilance inspection reports 6 (FOI-21-16)

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If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email [email protected]. Please tell us what format you need. It will help us if you say what assistive technology you use.

Pharmacovigilance inspection reports 7 (FOI-21-16)

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If you use assistive technology (such as a screen reader) and need a version of this document in a more accessible format, please email [email protected]. Please tell us what format you need. It will help us if you say what assistive technology you use.

Dioctyl pre-clinical and clinical expert report (FOI-21-026)

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Application for product licence (FOI-21-066)

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Assessment Report 1 (FOI-21-069)

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Assessment Report 2 (FOI-21-069)

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Updates to this page

Published 24 March 2021

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