Publication
“AI and sustainability - cure or curse?”
While AI can help resolve data issues in sustainable investing, it can create problems such as information breaches and inherent bias in data.
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
While AI can help resolve data issues in sustainable investing, it can create problems such as information breaches and inherent bias in data.
Publication
In this edition of Regulation Around the World we review recent steps that financial services regulatory authorities have taken as regards investment research.
Publication
The ongoing conflicts and further geopolitical tensions in Eastern Europe and the Middle East, coupled with upcoming elections in a number of key countries including the US and the UK, make 2024 challenging to predict what impact this will have on the insurance sector.
Subscribe and stay up to date with the latest legal news, information and events . . .
© Norton Rose Fulbright LLP 2023