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Register to vote Register by 18 June to vote in the General Election on 4 July.
Resources for public sector commissioners to help deliver public services.
Design, build and operate APIs in a consistent way
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Guides councils in preparing planning policies on housing for older and disabled people.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
Learn about legislation and insurance requirements for UK spaceflight.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Advises how to identify suitable mitigation and adaptation measures in the planning process to address the impacts of climate change.
Information on progress delivering the Inclusive Britain action plan.
Information on how we are growing the UK’s satellite launch capability and spaceflight industry.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Make sure your technology, infrastructure and systems are accessible and inclusive for all users.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
How to use a quasi-experimental study to evaluate your digital health product.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
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