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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to create a model of how your digital health product works and choose measures for your evaluation.
Resources for individuals and organisations to use supporting a variety of safety awareness campaigns.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
What you need to know about and do to comply with the law and keep consumers safe.
Things to consider when buying and using products.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
The campaign supports the IPO's commitments to raise public understanding, and ultimately respect, for IP rights.
How we are building national capacity for product safety.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
Compare different evaluation approaches and choose an appropriate method.
Research into consumer attitudes and behaviours in relation to product safety.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to use routinely collected data to evaluate your digital health product.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
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