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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.
Guidance for manufacturers, importers and distributors.
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.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How a marketing authorisation holder should report a defect with a veterinary medicine.
How to use an interrupted time series to evaluate your digital health product.
Using an ecological momentary assessment to evaluate your digital health product.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to use a quasi-experimental study to evaluate your digital health product.
Compare different evaluation approaches and choose an appropriate method.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Things to consider when buying and using products.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
How to use an ethnographic study to evaluate your digital health product.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
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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