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How to create a model of how your digital health product works and choose measures for your evaluation.
The duties and competence requirements for building regulations that clients, designers and contractors must meet.
Learn about about importing and exporting goods.
All essential shared data assets (ESDA) must be assessed for data quality issues, made findable and be available through APIs.
Finding the right advice and advisor is the first step in making the best decisions for your invention or business.
How to make an import declaration and get goods through the UK border.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The Building Safety Act 2022 created legal protections for leaseholders from historical building safety costs.
Tools to help schools assess their behaviour culture, recognise good practice and identify areas that need attention.
How developers can create and enhance habitat off-site or buy biodiversity units to achieve biodiversity net gain (BNG).
How to apply for national listing of agricultural and vegetable plant varieties in Great Britain and Northern Ireland.
Guidance on plan-making.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Find out what steps you need to take before you calculate how much you can claim for furloughed and flexibly furloughed employees.
Information for voluntary and community sector organisations (VCS) looking to responsibly make matches between sponsors and guests as part of the Homes for Ukraine scheme.
How to use the simplified declaration procedure when importing goods into the UK.
Webinars for pharmaceutical companies, clinical trial sponsors, e-cigarette producers and brokers of medicinal products
Find out about exercising due diligence when making customs declarations.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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