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Advena Awarded The Best Med-Tech Consultancy 2022

Following on from last month’s announcement of our nomination we were honoured to be awarded the prestigious title Best Med-Tech Consultancy for 2022. The award ceremony on the evening of November 18th, 2022, recognised so many companies and individuals who have made a positive contribution to our industry it was truly humbling to be part … Read more

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MDR / IVDR Article 13 Regulatory Importer Service

Advena Services Limited (ASL) is pleased to announce the launch of a much-needed service. Many clients who use Advena Limited as their EU Authorised Representative have asked on a number of occasions if we can also take on the regulatory responsibilities of Article 13. These previous requests have in the past been unfortunately declined due … Read more

Advena Launches a New Group Company

Advena Limited is pleased to announce the creation of a new Group Company, incorporated very recently in Malta and owned by Advena Malta (Holdings) Limited in the UK. We are therefore pleased to introduce Advena Services Limited (ASL). This new group company will take on new business that cannot be effectively taken on by its … Read more

Regulatory Consultancy – Technical File Creation, Gap Analysis / Reviews & Updates

Regulatory compliance is absolutely key to your success in both the EU and UK markets. As we all know, regulation is weighing down on manufacturers it is becoming costly and burdensome to handle in-house. Particularly since the EU has raised the standards for compliance with the introduction of Regulations (EU) 2017/745 & 2017/746. However, there … Read more

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MHRA Announce a 12-Month Extension to UK Medical Device Regulations

The MHRA recently published its intention to put into place a 12-month extension to the UK’s transitional arrangements. Currently, the UK MDR 2002 states that CE-marked devices will be accepted on the Great Britain (GB) market until the end of June 2023. However, this will now change. The MHRA will introduce an extension to the … Read more

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Advena Nominated for Best Med-Tech Consultancy 2022

The good news just keeps coming, in addition to the fantastic news of the Best Medical Device Regulatory Consultancy Award, we are also honoured to have also been nominated by Med-Tech World as the Best Med-Tech Consultancy for 2022. It seems to be a great year of recognition for Advena Limited in Malta. We will … Read more

Advena Awarded Best Medical Device Regulatory Consultancy 2022

AI Global Media Ltd has reached out to Advena to Award us with the prestigious title; Best Medical Device Regulatory Consultancy 2022. It is an honour to receive such an award and is a testament to the hard work, diligence, and desire to be excellent, not to mention the outstanding client reviews we receive. We … Read more

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MDCG Guidance on EU Authorised Representatives Released: MDCG 2022-16

This document is long overdue, however, here it is! The MDCG 2022-16 Guidance on Authorised Representatives concerning Regulations (EU) 2017/745 & 2017/746. It lays out what medical device manufacturers should expect as a minimum from their appointment EU Authorised Representative. There are some interesting elements of the Regulations explained and clarified as guidance and as … Read more

Advena is Taking Part in MED-TECH WORLD in Malta

As mentioned in previous editions of our monthly newsletter, Advena is taking part at MED-TECH World in Malta, it is a two-day trade show taking place on November 17th and 18th 2022. We welcome existing clients and those who wish to learn about how we can help with medical device compliance to visit us at … Read more

Concept of MDR Medical Device Regulation.

Manual on Borderline and Classification under Regulations (EU) 2017/745 AND 2017/746

September 2022 saw the release of this much-anticipated document, it records the agreements reached by the Member State members of the Borderline and Classification Working Group (BCWG) following the exchanges under the Helsinki Procedure under Regulation (EU) 2017/745 on medical devices (the MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR). This … Read more

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