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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.
Find out about the customs simplified procedure aggregation rules for the Customs Declaration Service (CDS).
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
An explanation of the offshore SEA process, including documentation of the most recent assessment and related consultation.
This document has been compiled to help local authorities that are interested in bidding for funding.
This collection page brings together government responses to investigation reports published by the Independent Inquiry into Child Sexual Abuse.
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
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