When doing business in Europe it is the manufacturer’s responsibility to carry out the conformity assessment with the European standards for its range of products. Since the introduction of the MDR (European Medical Device Regulation 2017/745) and the IVDR (European in Vitro Diagnostic Medical Device Regulation 2017/746 (EU-IVDR), we understand this process for medical devices and diagnostic products has far become more complex.This is the reason , we have invited BSI Business Development manager, who has been an auditor himself, Arjun Joshi to share his experience in taking Australian and NZ through this process.Your host for this session, Christelle Damiens will interview Arjun in this 20-minute Exportia LAB and the audience will have the opportunity to ask questions! BE AWARE this session will not be recorded.
info@wilam.comAn initiative ofBioMelbourne NetworkLevel 6, HWT Tower40 City RoadSouthbank, VIC 3006
Wilam means home in the Woi-wurrung language of the Wurundjeri People of the Kulin Nation, the Traditional Owners of the lands on which we are based.We respectfully acknowledge the Traditional Custodians of the unceded lands and waters of Victoria, the Bunurong, Eastern Maar, Gunaikurnai, Wadawurrung and Wurundjeri Woi-wurrung peoples, on which we live and work. We pay respect to their Elders past and present. We acknowledge the significant contribution that they and other Aboriginal and Torres Strait Islander people have made and continue to make to the research and knowledge systems that inform our community and our sector. We acknowledge that Aboriginal and Torres Strait Islander people continue to live in a spiritual and sacred relationship with this country and recognise our responsibility to continue to work towards reconciliation.