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Producer responsibility laws in the UK cover packaging, electrical and electronic equipment (EEE), batteries and end of life vehicles (ELVs).
Information on how to request assistance from NSDR.
What you need to know about and do to comply with the law and keep consumers safe.
How to use a before-and-after study to evaluate your digital health product.
How to create a model of how your digital health product works and choose measures for your evaluation.
Things to consider when buying and using products.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Product Recall for Unbranded Black and Orange Life Jacket presenting a serious risk of drowning.
How to use a cost effectiveness analysis to evaluate your digital health product.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Product Recall for Pink and Black Life Jacket sold via Amazon presenting a serious risk of drowning.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Our primary purpose is to protect people and places from product-related harm, ensuring consumers and businesses can buy and sell products with confidence. Office for Product Safety and Standards is part of the Department for Business and Trade .
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
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