Outsourcing in Clinical Trials: Medical Devices Europe 2016 16–17 February 2016, Munich, Germany

The two day programme features sessions designed to provide the tools for medical device companies of all sizes to use in a challenging market.

With a focus on developing comprehensive strategies that fit in with your business model, Outsourcing in Clinical Trials: Medical Devices Europe 2016 aims to mitigate risk in clinical trials at every stage of product development.

The event brings together industry figures from across Europe to provide insightful advice from years of experience implementing new ideas within the medical device sector.

The two day programme features sessions designed to provide the tools for medical device companies of all sizes to use in a challenging market.

Outsourcing in Clinical Trials: Medical Devices Europe 2016 has an extensive list of speakers from across Europe.

There are also two Eastern European speakers, which are Biosensors International Post-Marketing Surveillance and Vigilance associate director Marzena Bichalska and Novo Nordisk clinical research manager Géza Oszetheimer.

This is significant as previous events heavily focused on the Western European perspective so these speakers will be providing an Eastern European viewpoint.

Other industry expert speakers include:

  • St Jude Medical Clinical Affairs EMEAC vice-president Hindrik Robbe
  • BSI regulatory and clinical head Gert Bos
  • Johnson and Johnson quality and regulatory compliance manager, Monir El Azzouzi
  • BD WW senior clinical development manager Florence Schwarzenbach
  • Berlin Heart Clinical Science team leader Alexander Reiprich

The event provides the opportunity to share a wide variety ideas and knowledge and promises to be an important step in minimising risk in the medical device industry.

For more information please visit www.arena-international.com/omdteurope/

When registering, please quote the reference code MK-JDP.

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