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Combination Products Workshop – Regulatory Overview for Drug/Device Combinations and Drug/Companion Diagnostics

June 11, 2012

Pharma Development and Business

Hotel Bildungszentrum 21, Basel, Switzerland Sept 18, 2012 This one-day conference will provide delegates with an understanding of the regulatory framework for drug/device combinations and drug/companion diagnostics, taking into account the latest revision of the European medical device and in-vitro diagnostics (IVD) legislation. It will focus on the differences between device and pharma regulations and will highlight challenges facing manufacturers who operate on the drug/device borderline where it is not immediately obvious which regulatory framework applies. EVENT CODE:12120

Organized by:			DIA Europe
Invited Speakers:			Carole Burnier Regulatory Affairs Manager Novartis Consumer Health SA, Switzerland Shayesteh Fuerst-Ladani, MBA,MS Director SFL Regulatory Affairs and Scientific Communication, Switzerland

Deadline for Abstracts:			N/A

Registration:			DIA Europe Kuechengasse 16, Postfach 4002 Basel, Switzerland Phone: +41-61-225-51-51 Fax: +41-61-225-51-52 Email: DIAEurope@diaeurope.org
E-mail:			diaeurope@diaeurope.org

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