Page 4 - Authorised Representatives News Today : Breaking News, Live Updates & Top Stories | Vimarsana

Stay updated with breaking news from Authorised representatives. Get real-time updates on events, politics, business, and more. Visit us for reliable news and exclusive interviews.

Top News In Authorised Representatives Today - Breaking & Trending Today

Ardonagh Group expands into Australia with acquisition


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 country s 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 Australia.
Resilium will continue to be led by managing director Adrian Kitchin, who has overseen the business’ growth trajectory over the past five years, with GWP under management of over A$500 million in 2020, generating revenue of A$19 million for the financial year ending 30 June 2020. ....

New South Wales , United Kingdom , Gold Coast , David Ross , Resilium Bidco , Paul Lynam , Adrian Kitchin , Ardonagh Group , Broker Network , Authorised Representatives , Compass Networks , Mergers Amp Acquisitions , புதியது தெற்கு வேல்ஸ் , ஒன்றுபட்டது கிஂக்டம் , தங்கம் கடற்கரை , டேவிட் ரோஸ் , பால் லைனம் , தரகர் வலைப்பின்னல் , அங்கீகாரம் பெற்றது பிரதிநிதிகள் , திசைகாட்டி நெட்வொர்க்குகள் , இணைப்புகள் ஆம்ப் கையகப்படுத்துதல் ,

Ardonagh makes Australian move - Insurance Age


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 part of a corporate subscription are able to print or copy content.
To access these options, along with all other subscription benefits, please contact [email protected].
You are currently unable to print this content. Please contact [email protected] to find out more. ....

New South Wales , Gold Coast , Ardonagh Group , Authorised Representatives , Mergers Amp Acquisitionsm Ampa , புதியது தெற்கு வேல்ஸ் , தங்கம் கடற்கரை , அங்கீகாரம் பெற்றது பிரதிநிதிகள் ,

Register medical devices to place on the market


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 can be registered with the
MHRA.
The
MHRA will only accept registration of devices from manufacturers or UK Responsible Persons that have a place of business in the UK, or from Authorised Representatives based in Northern Ireland (for the purposes of the Northern Ireland market). ....

United Kingdom , Northern Ireland , Great Britain , Medical Devices Regulations , United Kingdom Responsible Persons , Authorised Representatives , Medical Device , United Kingdom Responsible Person , United Kingdom Responsible , Authorised Representative , Northern Ireland Based Authorised Representative , Kingdom Approved Body , Device Online Registration System , United Kingdom Authorised Representative , Public Access Database , Device Registration , Free Sale System , Free Sale , ஒன்றுபட்டது கிஂக்டம் , வடக்கு ஐயர்ல்யாஂட் , நன்று பிரிட்டன் , மருத்துவ சாதனங்கள் ஒழுங்குமுறைகள் , ஒன்றுபட்டது கிஂக்டம் பொறுப்பு நபர்கள் , அங்கீகாரம் பெற்றது பிரதிநிதிகள் , மருத்துவ சாதனம் , ஒன்றுபட்டது கிஂக்டம் பொறுப்பு நபர் ,

Regulating medical devices in the UK


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 Scotland.
For Northern Ireland, different rules apply to those in Great Britain. For more information on the regulatory system for medical devices in Northern Ireland, please see Regulation of medical devices in Northern Ireland below. ....

United Kingdom , Northern Ireland , Great Britain , Competent Authority , Vitro Diagnostics Association , Association Of Great Britain , Customer Services Centre , Regulatory Agency , Eu Competent Authority , Association Of British Healthtech Industries , Notified Bodies , United Kingdom Notified , Kingdom Notified Bodies , United Kingdom Approved , Northern Ireland Based Authorised Representatives , United Kingdom Responsible Person , Medical Devices Regulations , These Regulations , Devices Regulation , Diagnostic Medical Devices Regulation , Agreement Act , Independent Medicines , Medical Devices Safety Review , Medical Devices , United Kingdom Conformity Assessment , United Kingdom Responsible Persons ,