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Since, April 2024, the MHRA has been using Lorenz DocuBridge for eCTD management in product licence submissions. This change is part of the modernisation of the MHRA’s Legacy Systems and is one of the initial tools launched in the RegulatoryConnect...
Learn about about importing and exporting goods.
This guidance about notifying other landowners applies to planning, householder, minor commercial and listed building consent appeals.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to submit a proposal to UKDI
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
Changes to Practice Direction 36L and 36M come into force on 30 December 2019.
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