Page 6 - Authorised Representative News Today

Nikkiso Cryogenic Services has announced that Soletec has become the Authorised Representative and Service Partner for Nikkiso Cryogenic Services in Qatar.

The Goods and Services Tax Network (GSTN) has issued module wise new functionalities deployed on the GST Portal for taxpayers.

Guidance on how to licence electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.

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Hong Kong Exchanges and Clearing Limited and The Stock Exchange of Hong Kong Limited take no responsibility for the contents of this announcement, make no representation as... | April 11, 2021

From 1 January 2021, you will need to comply with the UK ETS as soon as you become an aircraft operator. This guidance will help aircraft operators understand and comply with their obligations under the The UK ETS applies to aircraft operators that were regulated by the UK under the European Union Emissions Trading System ( EU ETS). It also applies to those that will be new to regulation in the UK. If you need to comply with the UK ETS, you must monitor your aviation emissions for each sche...

United Kingdom: Impact of the EU-UK Trade Cooperation Agreement and Northern Ireland Protocol on life sciences Following four and a half years of often acrimonious negotiations and numerous build ups to a no-deal situation, the EU-UK TCA represents a positive step. While the deal is relatively thin and offers only discrete regulatory reciprocity, overall the TCA is a welcome development in the face of apparent near- political failure to agree on a way forward between the two sides. The life sci...

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...