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Register to vote Register by 18 June to vote in the General Election on 4 July.
Opportunity to license Dstl technology: a search manikin to aid forensic reconnaissance in the environment of drowning (FRED).
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
The tool is a major advance in how the IPO performs patent searches.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Information and guidance on a range of medical devices for users and patients.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Information about the qualifications available under the statutory digital entitlement.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Order a certificate of free sale to export medical devices outside the UK.
Practical steps to manage the risk of online harms if your online platform allows people to search user generated content.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Information about the EU Regulations and their implementation in Northern Ireland
Find registered patents, patent applications and pending patents
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How schools should setup a Microsoft Windows laptop or tablet before lending the device to a child, family or young person.
Form OS2: official search with priority by a purchaser against part of the land in a registered title or pending first registration application.
How to get fast-track approval of medical devices during COVID-19.
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