- email:registrations@informa-ls.com
- phone:+44(0)20 7017 7481
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6th Annual
Medical Device Directive and the Recast
25 - 26 January 2012
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Medical Device Directive and the Recast
Challenges imposed by the Medical Device Directive and the Recast clarified
Informa Life Sciences’ 6th annual Medical Device Directive conference is the first meeting where the European Commission presents the Recast porposal due to be published in the first quarter of 2012. It is the only event where you can quiz representatives from Member States and Notified Bodies by participating in an active panel session and hear their reactions to the Recast proposal. This conference is a must for regulatory affairs, quality assurance and all of those who are affected by the Medical Device Directive and the Recast.
The latest European Commission and industry updates on the status of Recast , recent developments and future trends within the EU medical device framework
- European Commission gives a critical overview of the Recast proposal and presents the results of the Impact Assessment read more
- Hear Eucomed's perspective on the Recast and its implications read more
- Gain insights into the latest progress made in achieving harmonisation between Notified Bodies read more
- Take part in an extended panel discussion on Recast read more
- 12 industry presentations and case studies read more
Expert Speaker Pannel
- Jacqueline Minor, Director for Consumer Affairs - European Commission, Health and Consumers Directorate-General
- John Brennan, Director of Technical and Regulatory Affairs, Eucomed, Belgium
- Niall MacAleenan, Pre-Market Evaluation Manager, Irish Medicines Board, Ireland
- Jan van Lochem, Vice President Healthcare – EMEA & Asia Pacific, BSI, UK
- Philippe Auclair, Senior Director, Regulatory Strategy and Advocacy, Abbott Quality and Regulatory EMEA, Abbott Vascular International, Belgium
- Chris Jepson, Global Manager – Medical Devices, SGS, UK
- Gert Bos, Head of Regulatory and Clinical Affairs, BSI, UK
- Peter Schröer, Director of Quality Systems and Regulatory Affairs, Ethicon Endo-Surgery GmbH, A J&J Company, Germany
- Joachim Wilke, Director Regulatory Affairs and Policy – Europe, Medtronic, Germany
- Alexander Geddes, Regulatory Affairs Director – EMEA, Boston Scientific, UK
- Anna Heile, Senior Clinical Research Scientist, Codman & Shurtleff, A J&J Company, USA
- Laura Locati, Regulatory Compliance & Quality System Director, EMEA, Abbott Vascular, Italy
- Torsten Kayser, Fellow Clinical Research Advisor, Boston Scientific, Belgium
- Mika Reinikainen, Managing Director, Abnovo Ltd, UK
- Jos van Vroonhoven,Radiation & Safety Manager - Quality, Regulatory & Sustainability, Philips Healthcare, The Netherlands
- Christoph Becker, Supplier Quality Manager, Zimmer, Germany
- Maurizio Suppo, Vice President - Standerdisation, Technology and Industry Affairs, Siemens AG, Siemens AG, Germany
Media Partners
Missed this event?
See what Farah Ramadan had to say about this event.
Farah Ramadan is an analyst within the IHS Healthcare & Pharma practice and attended this Conference in Brussels in January 2012. Read her comments HERE.Usability within the Medical Device Directive
PRE CONFERENCE WORKSHOP: TUESDAY 24 JANUARY
Usability requirements within the Medical Device Directive
An extensive and dynamic workshop where you can gain practical regulatory considerations for assessment and implementation of usability requirements.
Revised RoHS Directive
EVENING SEMINAR: WEDNESDAY 25 JANUARY 2012
Revised RoHS Directive and its impact on the Medical Device Directive
Take part in this insightful evening seminar where you will discover key issues that you need to be aware of with regards to revices RoHS regulations, and how it will impact the medical device manufacturers. After the seminar you will be able enjoy dinner and refreshments, providing a perfect opportunity for networking and speaking with leading experts.
Medical Devices in the CEE and the CIS including Russia
Post Conference Workshop: Friday 27 January
This workshop is highly interactive and is designed to educate you on regulatory affairs within Central and Eastern Europe (CEE) and the Commonwealth of Independent States (CIS), including Russia. Make sure you understand current procedures and are able to get to grips with these lucratice markets.
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Dates and Venues
25 Jan 2012 - 26 Jan 2012
La Plaza Hotel, Brussels, Belgium
Last year's delagate said...
"Good, relevant and very open discussions" Regulatory Affairs Senior Project Manager, Coloplast AS
"Exhaustive programme with good content of presentations", Regulatory and Compliance Manager, Abbott Vascular
