Page 2 - Authorised Representatives News Today

Access your UK Kyoto Protocol Registry account If you want to hold or trade Kyoto Units, you will need to have a Person Holding Account in the UK Kyoto Protocol Registry. From: The Kyoto Protocol to the United Nations Framework Convention on Climate Change ( UNFCCC) is an international climate change treaty which sets out emission reduction obligations for certain countries, including the UK. The first commitment period under the Kyoto Protocol ran from 2008 to 2012. A second commitment pe...

Ardonagh Group expands into Australia with acquisition 16-02-2021 04-09-2019 UK insurance intermediary The Ardonagh Group has expanded in Australia with the acquisition of Resilium BidCo, the countrys largest independently owned intermediary network. With offices in Sydney, Melbourne and the Gold Coast, Resilium connects a network of more than 150 Corporate Authorised Representatives (ARs) with over 100 insurers globally, providing business and personal insurance solutions to clients across Aus...

Insurance Age Subscriptions Subscriptions According to Ardonagh, Resilium is the largest independently owned intermediary network in the country. It has offices in Sydney, Melbourne and the Gold Coast, and connects a network of more than 150 Corporate Authorised Representatives (ARs) with over 100 insurers globally. Centrepiece  Group CEO David Ross said: “We’re thrilled to be welcoming Resilium into the Ardonagh portfolio as the centrepiece Only users who have a paid subscription or are p...

A loss in the NSW Supreme Court and action by the Australian Securities and Investments Commission has seen the Australian Financial Complaints Authority forced to change the way it handled complaints relating to authorised representatives.

Register medical devices to place on the market How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland From: Contents MHRA under existing arrangements: MHRA subject to grace periods, depending on the class of devices. In Great Britain devices must conform to the Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002) as they apply in Great Britain so that they ...

Regulating medical devices in the UK What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets. From: MHRA) is responsible for regulating the UK medical devices market. This guidance provides information on the UK system, including for: getting your device certified MHRA This guidance is divided into sections on the different rules that apply in Great Britain, Northern Ireland and the EU. Great Britain is England, Wales and Scotlan...