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Guidance for manufacturers, importers and distributors.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The GEO is the operating title of the United Kingdom’s military mission in Germany.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Keep systems and data safe with the appropriate level of security.
Find out how the GAAR Advisory Panel opinions are used by HMRC to decide whether tax arrangements are abusive.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This is collated guidance from government websites and independent bodies to help you follow the technology code of practice.
Options for amending proposals that have planning permission.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Pharmacovigilance system requirements
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
Responding to suspected breaches of planning control.
This page provide guidance for Civil Servants using the Evaluation Registry
Provides access to and updates on the status of existing and newly published National Infrastructure Planning Guidance.
Find the best guidance and tools to meet the accessibility regulations.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
Guidelines for civil panel counsel, revised to include the new government security classifications.
Keep up to date with the latest information from the UK GLP monitoring authority.
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