- email:registrations@informa-ls.com
- phone:+44(0)20 7017 7481
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Medical Device Design and Development
17 - 18 October 2012
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Informa Life Sciences Medical Device Design and Development Conference
Industry case studies on design and development, benchmarking design strategies and ensuring successful lifecycle management
Join us in London on 17-18 October for our exciting new event: Medical Device Design and Development - the first event of its kind in Europe - don't miss this opportunity to attend the only event whcih is specifically tailored to those working in medical device design.
At this event you will hear critical updates from industry and learn from important case studies to ensure your designs are successful for their entire lifecycle - from concept through to design transfer and post-commercialisation.
With field safety notices rising by over 1000% in the last 5 years, ensure your design processes are effectively minimising the risk of product recall!
Media Partners
Speakers include
Speakers include
Mike Hess
Vice President, Bradycardia R&D, CRDM Division
Medtronic
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Claus Geiger
Global Device Project Leader
Sanofi-Aventis
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Hagai Livni
Head of Software Validation
Given Imaging Ltd.
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Peter Bogaert
Partner
Covington & Burling LLP
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2012 Expert Speaker Faculty
- Mike Hess, Vice President, Bradycardia R&D, CRDM Division, Medtronic, USA
- Mathias Buerger, Vice President, Quality Assurance and Regulatory Affairs, Zimmer, Switzerland
- Lan Nguyen, Director, Quality Engineering, Edwards LifeSciences, USA
- Patrick Sauder, Director, Head of Corporate Design & Product Compliance, Institut Straumann, Switzerland
- Rikke Westergaard, Head of S&SI, Global Operations, Coloplast, Denmark
- Kathleen Whanger, Senior Biocompatibility Specialist, Boston Scientific, USA
- Claus Geiger, Global Device Project Leader, Sanofi-Aventis, Germany
- Dmitry Nikolaev, Lead Auditor/Expert, BSI Management Systems CIS, LLC, Russia
- Hagai Livni, Head of Software Validation, Given Imaging Ltd., Israel
- Ann Cooper, Engineering Design Manager, Summit Medical, UK
- Sanja Ilic, Chief Compliance Officer and Senior Vice President Clinical Regulatory and Quality Affairs, Banyan Biomarkers Inc. and President, CRQ Management Solutions, USA
- Peter Bogaert, Partner, Covington & Burling LLP, Belgium
- Dominic Furniss, Researcher Co-Investigator on CHI+MED, University College London, UK
- Shane Sayers, Partner, Head of Product Liability Department, Kennedy’s Law, UK
- Robert Johnstone, Board Member, International Alliance of Patients Organizations, UK
- Anne Ware, Partner, Kennedy’s Law, UK
- Paul Lafferty, Director and Principal Consultant, Medical Technology Consulting Limited, UK
- Ton Pennings, General Manager, CE Partner 4U, UK
- Barry Sands, President and Founder, RQMIS Inc., USA
This Conference is CPD Certified
The CPD Certification Service is the independent body operating across all market sectors and in support of all professional institutions, bodies and societies. Its certified CPD ‘quality mark’ is a recognised symbol of quality assured training. The prime role of the CPD Certification Service is to certify that the content of training courses, papers delivered at conferences and other educationally beneficial material conforms to universally accepted CPD guidelines.
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Event Workshops
Pre-Conference Workshop – Tuesday 16 October
Exploring Requirements for the Design and Development of Medical Devices in Key Global Markets
Evening Seminar Workshop - Wednesday 17 October 2012
The Role of Risk Management in Medical Device Design and Development
Post-Conference Workshop – Friday 19 October
Taking a Design from Concept to Commercialisation
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The CPD Certification Service
