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Quality assurance, Guarantee, Standards, ISO certification and standardization concept.

Breaking News! Intertek/AMTAC

It would seem Intertek have sent out co-ordinated information regarding their future certification activities, we have now heard from multiple sources and can confirm the following important information: Intertek has chosen to centralise its Notified Body activities to Intertek Semko AB (NB No 0413) in Kista, Sweden (SEMKO). This will lead to the closure of … Read more

Meet Advena at Arab Health 2018

Advena will be located in Hall 7, Stand H7C50 at this important show in Dubai from 29th January to 1st February 2018. We will be available to meet clients old and new during this trade show and have access to meeting room facilities at the ABHI UK Pavilion. We advise those who would like to … Read more

Due to Continued Growth Advena are Seeking to Employ Another Senior Regulatory Consultant.

Job description Role Title Senior Regulatory Consultant – Medical Devices Location Office Based in Warwick, United Kingdom Rewards Competitive salary. About Us Advena is essentially two companies; Advena Limited and Advena Medical Limited, both based at our offices in Warwick, UK. Both companies are expanding medical device consultancy business, Advena Limited also has an office … Read more

An Exciting Career Opportunity With Advena Limited

Job description Role Title Regulatory Associate – Medical Devices Location Office Based in Warwick, United Kingdom Rewards Competitive salary. About Us Advena is essentially two companies; Advena Limited and Advena Medical Limited, both based at our offices in Warwick, UK. Both companies are expanding medical device consultancy business, Advena Limited also has an office in … Read more

Concept of MDR Medical Device Regulation.

Reusable Surgical Instruments in EU Regulation 2017/745

A Reusable Surgical Instrument is defined as: “an instrument intended for surgical use in cutting, drilling, sawing, scratching, scraping, clamping, retracting, clipping or similar procedures, without a connection to an active device and which is intended by the manufacturer to be reused after appropriate procedures such as cleaning, disinfection and sterilisation have been carried out.” – … Read more

Categories MDR
Concept of MDR Medical Device Regulation.

Intended Use VS Indications For Use

Over the years, the amount of regulatory terminology seems to grow at a constant rate, and so it is no surprise that even the more fundamental terms start getting confused. We have seen many cases in which “Intended Use” and “Indications for Use” have been used interchangeably. Sometimes, “Indications for Use” are not even considered! … Read more

Categories MDR

Meet Advena at MEDICA 2017

Three members of our team will be visiting MEDICA 2017 in Düsseldorf this November. We are available to meet both new and existing clients – please email in advance to arrange an appointment at a convenient time. John Adcock Managing Director john@advena.mt Kenneth Shaw Regulatory Associate kenneth.shaw@advena.mt

Concept of MDR Medical Device Regulation.

Avoid This Major Non-Conformity

A Major UK based Notified Body recently issued a major non-conformity to a medical device manufacturer in South Africa.   The auditor was not satisfied with the arrangements in place between the manufacturer and their EU Authorised Representative (EC Rep), in particular that their EC Rep was not a member of the European Association of … Read more

Categories MDR
Miscellaneous

ISO 13485:2016 Success!

Advena Medical have chalked up a remarkable success, and at the first time of asking! Having read and understood the requirements of this new edition of the QMS standard. Advena’s experts set about this tricky task providing carefully planned advice and guidance to our client, the result of which, after a 3 day audit by … Read more

Concept of MDR Medical Device Regulation.

Gap Analysis to the new Medical Device Regulation EU 2017/745 (MDR)

This Regulation was released May 2017, the 3 years transitional clock is now ticking, manufacturers of medical devices have until May 2020 to be compliant. On first thought this appears to be plenty of time. However you should start your planning process now! Manufacturers across the world are not only planning to transition to the … Read more

Categories MDR
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