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How the Certification Officer (CO) applies her powers to act without a complaint to conduct investigations into trade unions and employers’ associations.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
This section of the SEPs Resource Hub provides an explanation of SEP specific words and terms used throughout the guidance.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Find out what makes a person an enabler of tax avoidance, and what to do about legally privileged communications.
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
Guidance on how UK government digital and technology spend control is applied within the context of the FCDO’s international development programming.
This guide provides information on how insolvency practitioners are authorised and regulated in Great Britain
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