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Information on the core components of the UK NQI, its four main institutions, and its impact on the UK national economy.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Frameworks which explain how to achieve end of waste status for certain waste derived materials.
How to use a cost utility analysis to evaluate your digital health product.
This research is part of the Gender, Growth and Labour Markets in Low-Income Countries programme
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Ensuring you get what you pay for.
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