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Did you mean appropriate product
How to create a model of how your digital health product works and choose measures for your evaluation.
Find out which sanitary protection products you can supply at the zero rate of VAT.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Guide for businesses on best practice when using non-disclosure clauses in compensation settlement agreements where product safety is a factor.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Compare different evaluation approaches and choose an appropriate method.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Intellectual property can be bought, sold or licensed.
How to use a cost effectiveness analysis to evaluate your digital health product.
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