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UK Government consults stakeholders on changes to UK REACH | Mayer Brown

On 16 May 2024, the UK Government launched an open consultation seeking stakeholders' views on various government proposals and policy options aimed at facilitating the transition of. ....

United Kingdom , Great Britain , Mayer Brown , United Kingdom Government , Great Britain Specific , Statutory Instrument , Safety Executive , Alternative Transitional Registration , Exit Implementation Period ,

SRUC scientist: 'Let them eat bugs' – with regulations in place

A SRUC academic is calling for GB regulation to be introduced for the sale and control of whole insects, and their ingredients, for human… ....

United States , United Kingdom , Northern Ireland , Great Britain , Pattanapong Tiwasing , Rebecca Sudworth , Innovative Knowledge Exchange , European Commission , Food Standards Agency , Food Standards Agency Or Scotland , Researcher Dr Pattanapong Tiwasing , Food Standards Scotland , Great Britain Specific , South American , Standards Agency , Policy Director ,

UK researchers to develop strategy for using edible insects in animal feed

Researchers at Scotland’s Rural College (SRUC) have been awarded funds to help develop a strategy for using edible insects in animal feed. ....

United States , United Kingdom , Northern Ireland , Pattanapong Tiwasing , Innovative Knowledge Exchange , European Commission , Food Standards Agency , Researchers At Scotland Rural College , Rural College , South American , Great Britain Specific ,

Apply for a licence to market a medicine in the UK

Apply for a licence to market a medicine in the UK
How to license a medicine for sale in the UK, including applications through national and international routes.
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This guidance also covers licensing a medicine in Northern Ireland through the centralised, decentralised and mutual recognition European procedures.
Which procedure to follow
There are several routes to obtain a marketing authorisation in the United Kingdom (UK), Great Britain (England, Scotland and Wales) or Northern Ireland. The options available will be determined by the intended market and the type of application. The markets in which each route is applicable are indicated in the following guidance: ....

United Kingdom , Northern Ireland , Great Britain , Canada Health , Committee For Medicinal Products , National Health Service , Regulatory Authority , National Rules Scheme , Department Of Health , European Union , Swiss Agency For Therapeutic Products Of Switzerland , Scottish Medicines Consortium , Food Branch , European Commission , Drug Administration , National Institute Of Heath Research , Council Of Europe , Community Procedures , Health Products , Group For Mutual Recognition , National Institute For Health , Health Research Authority , National Procedure , Health Sciences Authority , Access Consortium , Commission On Human Medicines ,