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Register to vote Register by 18 June to vote in the General Election on 4 July.
The CMA investigated the anticipated acquisition by Cochlear Limited of the hearing implants business of Demant A/S, known as Oticon Medical.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to conform with the legal requirements for placing medical devices on the market.
Order a certificate of free sale to export medical devices outside the UK.
How to register with an NHS doctor and patient questionnaires in Ukrainian and Russian.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information and guidance on a range of medical devices for users and patients.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
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.
Data First is a pioneering data-linking, research and academic engagement programme led by the Ministry of Justice and funded by ADR UK.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
Reapply for a driving licence if your licence was taken away (revoked) or if you surrendered your licence following a medical condition
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
We’re responsible for handling appeals against decisions by the Secretary of State for Education, the Secretary of State for Health, Care Quality Commission, Ofsted or the Care Council of Wales which exclude, remove or suspend you from a register to...
Information for patients, healthcare professionals and developers of new medicines
We’re responsible for handling applications for the discharge of patients detained in psychiatric hospitals. We also handle applications to change community treatment orders and the conditions placed on a ‘conditional discharge’ from hospital. Who we are We are part of...
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
When to tell DVLA about a medical condition or disability - what will happen to your licence, renewing or reapplying for your licence.
Don’t include personal or financial information like your National Insurance number or credit card details.
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