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JMDR Editorial Advisory Board Members to Speak at Upcoming Regulatory Events

London, 23 August 2007 -- Several Editorial Advisory Board members of the Journal of Medical Device Regulation (JMDR) are to attend important regulatory conferences throughout the second half of 2007:

Haroon Atchia, CEO & Technical Director, Quality First International Ltd, London, UK will be attending 'Topical Issues for Expert Witnesses' run by the Expert Witness Institute in London, UK on 18 September 2007.

Rainer Hill, Deputy Director General, BVMed, Berlin, Germany will be making a presentation on 'Changes in the Medical Device Legislation in 2007 - A Survey' at the Deutscher Medizinprodukte Recht Tag 2007 on 26 October 2007 in Frankfurt/Main, Germany. He will also be speaking about the 'Transposition of the Medical Device Law into Daily Practice: Industry Expectations' at a conference for BVMed members, Competent Authorities and press representatives on 7 November 2007 in Bonn, Germany.

Dr David Jefferys, Vice President, Global Regulatory, Eisai R&D Management Co Ltd, UK will be chairing a Management Forum meeting on combination products on 20-21 September 2007 in London, UK and will be attending the Regulatory Affairs Professionals Society (RAPS) Annual Meeting in Boston, MA, USA as the President-elect of RAPS on 23-26 September 2007.

Edward C Wilson, Jr, Hogan & Hartson LLP, Washington DC, USA will be speaking at the Medtec Ireland conference in Galway on 19 September 2007.

Meetings with JMDR Editorial Advisory Board members at these events can be arranged through Marija Capek, PR and Press (tel: +49 (0)621 1662326).

About 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. The full articles are only accessible to subscribers of the JMDR.

For further information

For more information on the Journal of Medical Device Regulation please contact Marija Capek at Global Regulatory Press, tel: +49 (0)621 166 23 26 or visit the Global Regulatory Press website at www.globalregulatorypress.com.

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