The 3rd Annual Sterilisation for Medical Devices
About The Event
Recieve practical advice from the experts to ensure efficient sterilisation and compliance with the latest standards: from cycle design to validation
Informa Life Science’s Sterilisation for Medical Devices conference is now in its 3rd successful year, helping professionals to navigate the problems and pitfalls encountered when putting together a sterilisation cycle. At this event you will have access to industry experts, both experienced device manufacturers and the regulators who write the standards. They will provide practical advice and expert opinions to help you fully comply with regulations and ensure your processes are running as efficiently as possible.
Event Highlights 2010
- Hear expert advice from 11 industry case studies read more
- Discover the value of working well with your contract steriliser read more
- Gain control of your bioburden analysis read more
- Debate the issues surrounding sterilisation of re-usable devices: read more
- Explore the potential of aseptic processing read more
- Review the relative merits of X-ray, E-beam and gamma sterilisation read more
Expert Speakers
Expert Speakers
Tony Faucette
Sterilisation Sciences
Stryker Orthopaedics, USA
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- Simon Redfern, Microbiology Manager, Smiths Medical International, Ireland
- Dr. Majella Geraghty, Certification and Inspections Officer, NSAI, Ireland
- C. Philip Cogdill, Corp. Director of Sterilisation & Microbiology, Boston Scientific, USA
- Thierry Wagner, Regulatory Affairs Manager EMEA, DuPont Medical Packaging, Luxembourg
- Sean Hanley, Corporate Manager, Sterilisation Department, Boston Scientific, Republic of Ireland
- Henry Sibun, Audit Team Manager, TUV Product Services, UK
- Carl Dover, Vice President of Worldwide Quality Systems, DePuy International Ltd., UK
- Stewart Brain, Microbiology Team Leader, BSI Healthcare, UK
- Ulla Christensen, Project Manager, Novo Nordisk, Denmark
Media Partner
Dates and Venues
23 Mar 2010 - 24 Mar 2010
Danubius Hotel Regents Park
Who should Attend?
Managers and heads of departments
Sterilization manager
Technical / Quality manager
Microbiologist
Virologist
Quality control
Validation Consultant
Engineering Design Manager
Process Engineer
Attendees to date
5 May 2010: New 1/2 day workshop
How to Manage an Outsourcing Transaction to Ensure Regulatory Compliance and Get Best Value
3 Key Sessions
- Outsourcing – A risk analysis
- Strategies to mitigate regulatory risks in outsourcing deals
- Strategies to minimise commercial risks and drive best value from an outsourcing transaction
Led by: Toby Crick, hazel Grant & Georgia Gavriilidou, Bristows
Poll
What is your greatest concern when designing a sterilisation cycle?
Please select an answer
Feedback from previous events
"Very well selected speakers from relevant companies for medical devices"
"A nice opportunity to be discussing with people struggling with the same problems – very inspiring discussions"
"Very high quality speakers and presentations in a superb environment"
