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Data, Freedom of Information releases and corporate reports
A complete list of 5G projects involved in the 5G Testbeds and Trials Programme
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
Find out what you should consider before using an umbrella company to make sure it complies with the tax rules.
Information about new applications, post-licensing, advertising, product information and fees.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
This guidance outlines how to create and implement a cloud strategy, and when to consider a single, hybrid or multi-cloud solution.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Lists of products using derogations under the European Commission Directive 2022/642
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
How HMRC deals with customers who are involved in tax avoidance, tax evasion or repeated insolvency who receive a joint and several liability notice, including how notices interact with penalties and safeguards.
Tell the CMA about competition and consumer issues.
How to license a medicine for sale in the UK, including national and international routes, and information on fees.
Like other forms of property, you can buy, sell and license IP, it is important you understand the value your trade mark, patent or design.
The VMR sets out the statutory fees associated with various regulatory services provided by the VMD. The statutory fees and fee structure are implemented from 17 May 2024.
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