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Scrip Regulatory Affairs
Regulating Medical Devices in Switzerland
14 January 2010
Karen Finn

Margit Widmann and Peter Studer of Swissmedic’s medical devices division talk to Karen Finn about how Switzerland’s unique role as an EU MRA contract partner affects its day-to-day regulatory activities.

It is well known in the international life sciences arena that Switzerland is a global leader in medical technology and the sector is growing at an increasingly fast pace...

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