4th Annual Labelling and Packaging Compliance for Medical Devices & IVDs
Europe’s Leading Two Day Labelling and Packaging Event
Informa LifeSciences’ 4th Annual Labelling and Packaging Compliance for Medical Devices and IVDs conference will deliver a comprehensive review of the global regulatory updates, and future developments for 2011. Through a combination of regulatory updates and practical advice into interrupting the requirements this conference is essential to ensure your current procedures remain compliant.
Gain vital advice from leading Medical Device and IVD companies
- Explore the current proposals for Alternative Delivery and E-Labelling for medical devices read more
Take away practical solutions for overcoming language requirements read more
Discover the latest initiatives for Unique Device Identification (UDI) and Bar-Coding read more
Examine the importance of the use of symbols read more
New for 2010! Participate in our interactive quick fire discussion forum on labelling requirements for emerging markets read more
Expert Speaker Panel
Expert Speaker Panel
Elena Varini, PhD
Regulatory Affairs Manager
Orthofix Srl - Italy
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Lucie Mattera
Regulatory Affairs Officer
EDMA
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Janice Kite
Traceability Director Healthcare
GS1 Global Office, Brussels, Belgium
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Plus:
- Joachim Wilke, Director Regulatory Affairs & Policy Europe, Medtronic
- Scott Mathis, Senior Director, Global Product Labeling, Siemens Healthcare Diagnostics Inc., USA
- Virginia Serra, Regulatory Affairs Specialist, Ethicon Endo-Surgery
- Holger Most, Regulatory Affairs EMEA, Kimberly-Clark Healthcare
- Bianca Gravenhorst Greve, Regulatory Affairs Manager, Coloplast A/S, Denmark
- Michael Grimm, Senior Packaging Engineer, Synthes, USA
for full details of the complete speaker faculty 2010 click here
Sponsors
Exhibitors
Promotional Participant
Media Partners
Dates and Venues
20 Oct 2010 - 21 Oct 2010
Holiday Inn London - Regents Park
Co-Located Event
The 5th Annual
Pharmaceutical Labelling & Packaging Conference
20 Oct 2010 - 21 Oct 2010
Holiday Inn London - Regents Park
The essential event for all those working in Labelling, Regulatory Affairs, Packaging, Quality Control & Translation.
Past attendees include:
- Labelling Manager
- Corporate Regulatory Affairs Department
- Labelling Translations Tech Support Department
- Regulatory Affairs Europe
- Regulatory Affairs CoE IV-Systems Department
- Regulatory Affairs Department
- Packaging Department
- Documentation Manager
- Quality Systems & Regulatory Affairs Department
- Corporate Labelling Project Manager
- Technical Publications Department
Practical Solutions to Label Design
Evening Seminar: 20th October 2010
Practical Solutions to Label Design
This will be a highly interactive practical seminar in order to establish solutions and best practices to designing a label for medical devices and ivds. The seminar will highlight regulatory and compliance issues related to designing correct and compliant labels taking into consideration, the updated regulations, label size, single use devices, multi-language labels, use of symbols and much more. Participants will work on selected case studies based on real life examples which will help them gain an understanding of how to design legible and user friendly labels while ensuring regulatory compliance.
Some of the issues being addressed will include:
- Designing a label for regulatory compliance
- Product size considerations for label design, designing a label for small, medium and large medical devices
- Labels for single use devices
- Managing multi-language labels and ensuring correct translation
- Correct use of symbols
- Case study examples of successfully designed labels for a series of product types
Seminar Leader: Dr Salma Michor, CEO and Principal Consultant, Michor Consulting EU, Austria
Media Partners
Reviews of 2009's event
"Very informative and helped hearing how new regulations we heard about last year have become tangible. Good for both RA and departments that actually create labelling. Very well combined."
"This conference is a must for package labelling project managers who want to stay up-to-date on changes in global package labelling compliance for medical devices"
