LRQA will once again be taking part in the ABHI Annual Regulatory Conference on 25 November 2014 in London.
The European Commission has suggested proposed changes to Medical Device Regulation (MDR) that will support transparency in the regulation of medical devices, tractability of devices and information on quality and safety of devices on the market.
This conference will bring you up-to-the-minute news as the final deliberations in the Council (Member States) and ongoing negotiations between the Council, the reconstituted Parliament and Commission, as well as what to expect next.
This is your opportunity to learn more about policy makers' future plans and prepare for the new requirements, as well as network with delegates from the medical sector.
Topics covered include UDI, labelling, reprocessing and sterilisation, clinical evidence, responsibilities of economic partners, own brand labelling and classification.
LRQA's industry expert Martin Penver, Head of Notified Body for Medical Device Directives, will be presenting on the following topic at the event:
Presentation: How key elements in the MDR will affect you - Notified Body Perspective
Date: 25 November 2014
Time: 12.15 - 12.45
LRQA will also be attending the table top exhibition and showcasing its range of Medical and In-Vitro Diagnostic Devices and Directives Services, including:
- ISO 13485 Certification
- Conformity assessment under IVD directive
- Conformity assessment under Medical device directive
- Training courses
To discuss your individual needs and how LRQA can help you meet your regulatory requirements,
To find out more about the event or register to attend, please visit ABHI