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EU Commission Release Report from Study Conducted Regarding the Implementation of Article 17 of Regulation (EU) 2017/745 on medical devices on the EU market

The EU Commission has released a report from a study that they have conducted concerning the reprocessing and reuse of single-use-devices in the EU. The study aimed to evaluate how the provisions that have been established in Article 17 of the MDR, which regulates the reprocessing of Single Use Devices (SUD’s), have been implemented and … Read more

Concept of MDR Medical Device Regulation.

MDCG 2024-5 guidance on content of the Investigator’s Brochure for clinical investigations of medical devices

The MDCG has released a guidance document concerning the content of the investigator’s brochure for clinical investigations of medical devices. For some background, when a sponsor of a clinical investigation submits an application in accordance with article 70(1) of the MDR, the application shall be accompanied by the documentation referred to in Annex XV, Chapter … Read more

Concept of MDR Medical Device Regulation.

MDCG 2024-4 – Safety reporting in performance studies of in vitro diagnostic medical devices under Regulation (EU) 2017/746

The MDCG has published a guidance document concerning safety reporting in performance studies of in vitro diagnostic medical devices under the IVDR. For some background, safety reporting in performance studies of IVD’s shall be performed in line with the requirements of Article 76(2) of the IVDR. According to Article 76(2) of the IVDR, the sponsor … Read more

Concept of MDR Medical Device Regulation.

Two New Notified Bodies have been Designated for MDR

April sees the addition of two new notified bodies designated under the Regulation (EU) 2017/745 (MDR). The notified bodies are from Denmark and France and are listed below: NB 2443: TÜV SÜD Danmark NB 0333: AFNOR Certification These new additions bring the total number of notified bodies designated under the MDR to 46. More information … Read more

Meet Advena at Hospitalar 2024

We are pleased to announce that we will be visiting Hospitalar in Sao Paulo from the 21st to the 24th of May. This is our first trip to Latin America, and we are very excited to meet some of our existing clients as well as many new prospective clients during this important medical fair. Our … Read more

Concept of MDR Medical Device Regulation.

New Notified Body has been Designated for MDR

March sees the addition of a new notified body designated under the Regulation (EU) 2017/745 (MDR). The notified body is from Sweden and is listed below: This new addition brings the total number of notified bodies designated under the MDR to 44. More information regarding this new notified body can be found using the following … Read more

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Advena at Medical Fair India

Earlier this month, our regulatory associate, Sam Attard, attended Medical Fair India in Mumbai on behalf of Advena. During this exhibition, Sam has met a number of existing clients as well as new potential clients that needed help with CE marking their medical devices. This is the first time Advena has visited an event in … Read more

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Two New Approved Bodies Announced by the MHRA

LNE-GMED (8521) and Scarlet (8536) have just been given approved body status by the Medicines and Healthcare Products Regulatory Agency (MHRA). These new additions bring the total number of UK approved bodies to 9. The full scope of LNE-GMED can be accessed using the following link The full scope of Scarlet can be accessed using … Read more

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Advena at Arab Health 2024

As many of our readers are aware, earlier this month, Advena participated at Arab Health Medical Trade Fair. Arab Health is considered to be one of the biggest Medical Trade Shows in the Middle East and saw a total of 3,450 companies exhibiting and a further 110,000 visiting in this year’s edition of the trade … Read more

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