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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidance for manufacturers, importers and distributors.
How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
The information required by the Regulator of Social Housing and the deadlines for submission.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
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