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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
When a material is waste, is a by-product or meets ‘end of waste’ status.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance for manufacturers, importers and distributors.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
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 object to an application to use or change a traditional term for a wine product on the UK traditional terms register.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Things to consider when buying and using products.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
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