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Data, Freedom of Information releases and corporate reports
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Standardisation explained.
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
Search for companies that can do Disclosure and Barring Service (DBS) checks on your behalf (formerly Criminal Records Bureau (CRB) checks)
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What we check and how you apply for approval.
Find out how the accessibility monitoring methodology is used to test websites and mobile apps under the Accessibility Regulations
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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.
We’re a unit located within core-Defra that supports Defra and the Scottish, Welsh and Northern Ireland governments and their paying agencies to administer the Common Agricultural Policy (CAP) in the UK in accordance with the UK’s Withdrawal Agreement with the...
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
An explanation of the offshore SEA process, including documentation of the most recent assessment and related consultation.
The Tribunal Procedure Committee makes rules governing the practice and procedure in the First-tier Tribunal and the Upper Tribunal. TPC is an advisory non-departmental public body, sponsored by the Ministry of Justice .
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Public Health England commissioned review on the impact of smoking on musculoskeletal system, cognitive function, oral health and vision.
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
Find out about local procedures, burials and cremations, and returning the body to the UK.
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