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Guidance for businesses and organisations on the relationship between trade marks and geographical indications (GIs) at the end of the transition period.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
The European Trade Mark and Design Network has updated its common practice on the general indications of the Nice classification headings in accordance with European Union Trade Mark Regulation No. 2015/2424.
The European Trade Mark and Design Network has updated its common practice on the general indications of the Nice classification headings. This is in accordance with the Nice Classification List (10 -2016).
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Use a separate statement of objection form for each Japanese GI product name you object to.
The Government's summary of an EU proposed regulation relating to geographical indications for wine, spirit drinks and agricultural products.
Find out about the Spirit Drinks Verification Scheme if you produce a UK spirit drink with a protected Geographical Indication.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
The Government's summary of an EU proposed regulation on geographical indication protection for craft and industrial products.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without an authorisation.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
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