Publication
UK Carbon Border Adjustment Mechanism: how will it work?
In February, we reported on the Department of Energy Security and Net Zero’s confirmation that a UK Carbon Border Adjustment Mechanism (CBAM) would be bought into force by 2027
Global | Publication | March 2017
In the European Union (EU), inspections of medicines manufacturing sites are carried out by national competent authorities from EU Member States. Each year, EU competent authorities and the US Food and Drug Administration inspect many manufacturing sites in the EU, US and elsewhere in the world, to ensure compliance with Good Manufacturing Practice (GMP).
EU and US regulators have agreed to recognise inspections of manufacturing sites for medicines conducted in their respective territories. The agreement is underpinned by an assessment that the EU and US have comparable regulatory and procedural frameworks. In future, the need for an EU regulator to inspect a site located in the US, or vice versa, will be limited to exceptional circumstances.
The agreement is an annex to the EU-US Mutual Recognition Agreement (MRA). Many provisions of the agreement have already entered into force and others will enter into force on 1 November 2017. The EU has existing MRAs of GMP inspections for several other countries including Canada, Australia, New Zealand, Japan and Switzerland.
Publication
In February, we reported on the Department of Energy Security and Net Zero’s confirmation that a UK Carbon Border Adjustment Mechanism (CBAM) would be bought into force by 2027
Publication
International financial markets have started to show significant interest in nature and biodiversity. Whilst climate change and greenhouse gas emissions have made the headlines in recent years, there has been much less focus on their equally important counterparts, nature and biodiversity. However, that has started to change.
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