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This page provides technical advice on the consideration of scope in the Environmental Impact Assessment Process for solar Nationally Significant Infrastructure Project (NSIP) development.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Check when packaging is classified as a finished plastic packaging component, and what is meant by substantial modifications, to find out if you must register for the tax.
Guidance on the various types of modifications that can be made to a clinical trial approval.
How to enforce copyright when somebody uses your work without your permission.
Employment Appeal Tribunal Judgment of Judge Auerbach on 6 February 2026.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance primarily aimed at local responders covering some humanitarian issues that may arise during the recovery phase of an emergency in the UK.
How investigators and sponsors should manage clinical trials during COVID-19
This list of commonly used terms is intended to assist persons who are affected by an application under the Planning Act 2008 who may be unfamiliar with the language used to describe aspects of the process.
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