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Sam Attard

Concept of MDR Medical Device Regulation.

Update of the Q&A Document on the Extension of the MDR Transitional Period

The initial document of the Q&A, released in late March, provided guidance for the amendment to the extension in transitional provisions. This document was well received by many entities within the regulatory space. There has been an update to the Q&A document that has been released in mid-July. The document conveniently includes a change history … Read more

Categories MDR

Meet Advena at Med-Tech World 2023

We are pleased to announce that we will be exhibiting at this years edition of Med-Tech World. The exhibition will be held on the 19th and 20th of October 2023 at the Mediterranean Conference Centre in Valletta. If you are interested in one of our services, or you are an existing client who would just … Read more

Medical instruments used by doctors

Update on Guidance MDCG 2020-3 Rev.1

The conditions that are set out in Article 120 (3) of the MDR include, among others, that legacy devices must continue to comply with the AIMDD/MDD, as applicable, and that there are no significant changes in the design or intended purpose of the device. The latter criteria could be considered as quite vague and could … Read more

Categories MDR

Advena Services Limited Obtains ISO 13485:2016 Certificate

We are pleased to announce that Advena Services Limited has successfully obtained their ISO 13485:2016 certificate from the Italian Notified Body IMQ, under the scope of MDR/IVDR Article 13 Regulatory Importer Service. Additionally, Advena Limited were also re-certified under ISO 13485:2016 by IMQ, under the scope of European Authorised Representative service, quality management, regulatory affairs … Read more

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