23 April 2009 : 2008 Seminar in Tel Aviv, Israel

In reference to the expected changes in the European Directives, Obelis initiated a seminar in Tel Aviv at the Israeli Export Institute on June 22nd. The seminar was a great success with over 50 participants in attendance.

The seminar focused on guidelines for the first implementations of the RoHS Directive 2002/95/EC and WEEE Directives 2002/96/EC & 2003/108/EC (Waste of Electric & Electronic Equipment) and the new amendment to the MDD 93/42/EEC, the 2007/47/EC and the influence of the Machinery Directive 98/37/EC and its amendment the 2006/42/EC on Medical Devices.

• Over 85% of the attendees stated that the main subjects of the seminar were relevant to their business & professional needs.

• Over 90% of the attendees found the speakers to be of high quality. In addition, the presentation given by Dr. Peter Ruys, Senior Regulatory Expert for Obelis was reviewed in the highest of regards.
If you would like to learn more about the important information provided at the seminar, a book containing the printed versions of the PowerPoint presentations from each of the 7 speakers is available for purchase for 400 ILS; Obelis clients will be able to purchase it at a discounted rate. To purchase this book, please contact us.

Details of the workshop as follows:
• Name: Latest Changes in European Directives for Medical Devices and new implementation of European “Green” Regulation
• Date:  June 22nd, 2008
• Time: 8:15 – 18:00
• Location: 5th Floor, Hall of Israel, The Export Institute of Israel, 29th Ha-Mered St., Tel Aviv, Israel
• Fee: 400 ISL

Agenda:

8:15-9:00 Registration
9:00-10:00 Mr. Amir Inbar – Mediclever
10:00-10:45 Roxanne Carter, WEEE Expert for Obelis
10:45-11:00 Break
11:00-11:45 Dr. Peter Ruys, Senior Regulatory Expert for Obelis
11:45-12:15 David Furst – Israeli Export Institute                                                                              
                      “The Map of Business Opportunities for the Israeli Life Science Industry”
12:15-13:00 Ariella Bardach and Sharon Mendlebaum – Mixun                                            
                      “CE Marking – From Strategic Planning to Full Implementation” 
13:00-13:45 Light Lunch
13:45-14:30 Dr. Ornit Yanay-Kohelet – Q Trials                                                
                      “Clinical Trials – Requirements and Process”
14:30-15:00 Segal Weisswaser – TBN Group                                                  
                      “Significance of Regulations to Marketing” 
15:00-15:15 Break
15:15-18:00 B2B Meetings    

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