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Cordis RA expert Elena Jugo joins Editorial Advisory Board of Journal of Medical Device Regulation

London, 5 February 2007 -- The Editorial Advisory Board of the Journal of Medical Device Regulation (JMDR) announced today the appointment of Elena Jugo from Cordis Corporation.

With 20 years experience in the clinical research, regulatory affairs and quality assurance fields, Elena Jugo currently holds the position of Manager of Regulatory Affairs in Cordis Corporation. Elena joined Cordis 12 years ago as a Quality Assurance Auditor. Later she transferred to the Regulatory Affairs department where she has managed several programmes in the endovascular division, ranging from catheter sheath introducers to endovascular stent grafts for the treatment of abdominal aortic aneurysms, and combination stent/drug devices. During this time her responsibilities have included product registrations in the USA and the European Union, as well as supporting affiliate countries all over the world to gain approval of Class II and Class III devices.

On the Journal of Medical Device Regulation

The Journal of Medical Device Regulation is intended to educate, provide professional guidance, develop core competence of regulatory professionals, and promote debate on fundamental and topical matters within the medical device industry. In addition to publishing review and discussion articles by opinion leaders from the device community, the Journal summarises the news headlines from around the world and provides useful reference information in the form of charts and briefing documents. The Journal is a quarterly, subscription-only publication which is currently only available in electronic format.

For more information

Please contact Marija Capek, PR and Press Officer, phone number +49 (0) 621 16 623 26 or visit the Global Regulatory Press website at www.globalregulatorypress.com.

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