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Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Explanation of terms used in Ofsted's official and national statistical releases.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
How to use an economic evaluation to evaluate your digital health product.
The Crown Commercial Service technology service principles help us to continually improve the way technology is bought across government and the public sector.
The Regulator of Social Housing publishes assessments on how well registered landlords are meeting regulatory standards.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Advice for manufacturers of Class I medical devices for placing products on the UK market
What is expected of a registered apprenticeship training provider.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidance and information for independent providers of NHS healthcare services.
Work and Health Programme provider memos.
These published standards relate to a number of KPIs in the VMD Deliverables and KPI document.
Actions that trial sponsors should consider to build resilience into clinical trial design
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