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Advena Limited – Statement on COVID-19

The COVID-19 pandemic is rapidly affecting lives and how businesses operate worldwide. Increasingly governments are introducing stricter measures to protect public health, which ultimately impacts on the movement of Advena Limited’s employees’, the individuals we trust to implement our regulatory obligations. During these difficult times the safety and well-being of our families, friends and colleagues … Read more

Concept of MDR Medical Device Regulation.

Unique Device Identification (UDI) System EU2017/745 & EU2017/746

The EU’s medical device regulations 2017/745 and 2017/746 require that each device placed on the market must be accompanied by a unique device identification (UDI) which shall be used for identification and traceability purposes. Note, this requirement applies to all devices apart from custom-made and investigational devices. The above is the proposed symbol to be … Read more

Come and Visit Advena at Arab Health 2020

At this year’s event both Advena Limited (UK) Advena Limited (Malta) will be represented. We will be located in Hall 2 Stand G15 within the UK pavilion, at this important show in Dubai from 27th to 30th January 2020. Please do come and visit to discuss your medical device regulatory needs, whether this be our … Read more

Miscellaneous

An Exciting Career Opportunity With Advena Limited in the UK

Due to continued growth Advena are seeking to add to our team of regulatory specialists, we have a new position available for those who meet the criteria outlined below; Role Title: QMS & Medical Device Regulatory Consultant. Location: Office Based in Warwick, United Kingdom. Rewards: Competitive salary. About Us: Advena is essentially two companies; Advena … Read more

Come Visit Advena at MEDICA 2019

Advena will be located in Hall17, Stand 17B16 – 7 at this important show in Dusseldorf, from 18th to 21st November 2019. We will be delighted to meet existing and prospective clients during this trade show. To meet one of our team we would encourage you to email us for an appointment, well in advance … Read more

Miscellaneous

An Exciting Career Opportunity With Advena Limited in Malta

Due to continued growth Advena Limited are seeking to add to our team of regulatory specialists, we have a new position available for a person who can meet the criteria outlined below; Role Title: Regulatory Associate – Medical Devices Location: Office Based in Swatar, Malta Rewards: Competitive salary. About Us: Advena Limited is essentially two … Read more

Concept of MDR Medical Device Regulation.

Medical Device Reclassifications or Up-Classifications: Devices that Currently do not Require a CE certificate

There are several devices that currently do not require a CE certificate under the Directives, which will need certification under the EU MDR by 26 May 2020 for continued market access. This may be due to up-classifications (e.g. some software that is currently Class I under MDD but are Class IIa or higher under MDR) … Read more

Concept of MDR Medical Device Regulation.

BREXIT UPDATE! UK & Non-UK Based Medical Device Manufacturers

As many of you will now know, the Conservative & Unionist Party have elected a new leader in Boris Johnson, who has also become the UK’s new Prime Minister. The new Prime Minister has clearly laid out his plans for the timetable of Brexit, in as much as that he and his team of cabinet … Read more

Categories MDR
Concept of MDR Medical Device Regulation.

UDI Issuing Entities

In early June, the European Commission (EC) announced the four issuing entities for the Unique Device Identifier (UDI): GS1, the Health Industry Business Communications Council (HIBCC), ICCBA Informationsstelle für Arzneispezialitäten (IFA GmbH). The decision was made with the help of the Medical Device Coordination Group (MDCG) after the four companies were found to meet all … Read more

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