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Register to vote Register by 18 June to vote in the General Election on 4 July.
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 apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information on designs hearings including costs and how to appeal against an outcome.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Guidance for local authorities and fire and rescue services on the use remediation orders, a Building Safety Act 2022 enforcement power.
Check the tariff classification for preparations put up for retail sale.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
Introducing the new pre-application service for Nationally Significant Infrastructure Projects.
Intellectual property research publications commissioned by the Intellectual Property Office (IPO) covering designs.
Volume 53 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Notices of publication and a consolidated list of references of pre-Exit European Assessment Documents for construction products.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
A guide to documenting how you’ve collected your packaging data, known as your ‘methodology’. Online marketplaces affected by extended producer responsibility (EPR) for packaging must submit a methodology. This is also recommended for all producers as part of their ways...
SEPs are of growing importance to the UK economy. The IPO is committed to ensuring the current SEPs framework functions effectively to encourage innovation and promote competition.
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