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Register to vote Register by 18 June to vote in the General Election on 4 July.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Information on the core components of the UK NQI, its four main institutions, and its impact on the UK national economy.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Guidance on the Quality Matters initiative, which aims to improve the quality of adult social care.
Quality reports pull together key information showing how the various dimensions of quality have been considered.
Information about Universal Credit statistics quality.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Proficiency testing (PT), also known as external quality assessment (EQA), allows the introduction of samples of known but undisclosed content into a laboratory’s routine testing procedure.
Delivery of substantial industry placements in return for industry placement capacity and delivery fund (CDF) in 2018 to 2019.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Check a list of recent emails from HMRC to help you decide if the email you've received is a scam.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Standardisation explained.
Anti-choking devices are intended to alleviate choking incidents after Basic Life Support protocols have been attempted and failed. There are numerous counterfeit and unbranded anti-choking devices being sold in the UK online which do not have a valid UKCA or...
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
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