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bioPmed, in collaborazione con Verum,
“Clinical trials of Pharma and Med-Tech products:
opportunities in Europe.”
07 Maggio 2014
Mercoledì 07 Maggio 2014
Ore 14.00 – 17.00
Seminario “Clinical trials of Pharma and Med-Tech products:
opportunities in Europe”
An essential step of the development for a new pharma or medical device is the approval by
regulatory authorities. This interactive workshop provides you a roadmap to successfully navigate
through the European regulatory environment and gives you the basis to successfully bring your
product to the market.
1. Introduction of Verum and CTL, a CRO and its logistic company for Medical Device, Pharma
and Biotech companies;
2. Overview of the regulatory environment at European level and some neighbouring
3. CE registration in EU;
4. Differentiation and combination of Medical device and Pharma, medical device and
nutrition, medical device and cosmetics;
5. Clinical trials – a must-have or an opportunity and advantage?
PD Dr. Jörg Schierholz, Verum, Medical Consultant for Medical Device
Dr. Dagmar Siebold, Verum, Director Client Relations
I seminari si svolgono presso la sede di Bioindustry Park Silvano Fumero
Via Ribes, 5 - 10010 Colleretto Giacosa (TO)
Il workshop sarà tenuto in lingua inglese
• Associati bioPmed: gratuito
• Non associati bioPmed: 50 euro
Occorre iscriversi 5 giorni lavorativi prima della data del seminario, sulla pagina “Eventi” del sito
Silvia Lepore, [email protected]
Marco Piunti, [email protected]
Tel. 0125/561311