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Advice for building professionals involved in school building projects.
Regulatory Policy Committee opinion on BEIS' Ecodesign and Energy Labelling for Lighting Products IA
Find out what Business Premises Renovation Allowance (BPRA) is and what costs and buildings qualify for it.
Product Recall for Lighting Equipment sold by Dream Home Store presenting a risk of electric shock.
The Lighting Study examines high and low users of lighting, lighting modelling, projections, potential efficiency savings and outdoor lighting.
Provides guidelines on the requirements and performance standards, for new technology light sources as required by the IMO.
We're seeking views on proposed updates the existing ecodesign and energy labelling requirements which currently apply to light sources and separate control gears ('lighting products') in the UK.
Official Government Buying Standards (GBS) for electrical goods: ovens, dishwashers, refrigeration units, washing machines, tumble dryers.
The daily Points of Light award recognises outstanding individual volunteers - people who are making a change in their community.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
A toolkit for manufacturers and suppliers with ETL compliant lighting products.
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Official Government Buying Standards (GBS) for construction/refurbishment projects and products: heating, lighting, taps, paint, timber etc.
Dstl exploits the latest in robotics and AI to create effective and trustworthy uncrewed platforms and autonomous systems for the UK’s security and defence.
This is a list of all the opinions the RPC issued in 2021 on Department for Business, Energy and Industrial Strategy measures.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance for manufacturers, their authorised representatives and importers.
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