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Year 2007

October

Come and meet us at the Medica exhibition between 14 and 17 November 2007

The MEDICA exhibition will be held in Düsseldorf, Germany, from 14 to 17 November 2007. With over 137 000 professionals from all over the world visiting in 2006, MEDICA has become the event healthcare companies cannot miss.

October

Achieving Medical Device Approval in Europe, 28 and 29 November 2007

Organised by Informa Life Sciences on 28 and 29 November in Boston, USA, this conference introduces the differences between American and European regulations, as well as the evolution of the latter. Role and responsibilities of the Competent Authorities and the Notified Bodies, technical documentation, clinical data, post-marketing surveillance are amongst the topics covered.

October

Second Annual FDA Inspections Summit, 22 to 24 October 2007

Organised by FDA news from 22 to 24 October in Bethesda, Maryland (Washingotn DC), in the USA, this congress aims at helping healthcare and medical decision makers get familiar with current regulations in the US, their evolution, and provides guidance on how to prepare for inspections.

September

The access to the Taïwanese market is facilited for Swiss medical devices manufacturers since July 4th, 2007

The swiss manufacturers of medical devices can call on LNE to facilitate their access to the Taïwanese market.

September

Some news related to the access of medical devices on the Australian market

In order to create certainty of supply of medical devices, the Australian authorities have passed the Therapeutic Goods Amendment Bill 2007 (modification of Therapeutic Goods Act 1989 (article 9B(2)) with a new transition deadline arrangements, which take effect from 3 October 2007.

May

G-MED North America present at OMTEC 2007

G-MED North America is participating in OMTEC 2007 (Orthopaedic Manufacturing Technology Exposition & Conference) on 20-21 June 2007 in Rosemont, Chicago.

February

LNE/G-MED is involved in the Pilot Multipurpose Audit Program (PMAP)

LNE/G-MED is involved in the Pilot Multipurpose Audit Programm (PMAP) developped by FDA (USA) and Health Canada. LNE/G-MED can be requested by medical devices manufacturers to carry out simultaneously :

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