13 Mar 12
- 15 Mar 12
The MEDTEC Europe conference is the biggest annual event for medical device manufacturers. Join other senior medical device professionals in Stuttgart (Germany) on 13-15 March 2012 to learn about and discuss best practice in product development, regulation and market access of devices.
With six tracks over three days you will hear vital advice and guidance on Health Technology Assessment, Pricing & Reimbursement; Human Factors Engineering; How to take your Device to the USA; Device Design & Quality; Risk Management and Testing; and the New Emerging Regulatory Environment.
The conference :
- Case studies by industry professionals
- Live debates, interactive panel discussions and roundtable brainstorms
- Exhibition with 1000+ exhibitors over 16,000sqm in 4 halls
Expert speakers include:
- Dr Marco Marchetti, Technology Assessment Unit, General Hospital Management
- University General Hospital Agostini Gemelli
- Dr. Gabriela Soskuty, Vice President, Government Affairs, Health Policy and Economics, B. Braun Melsungen AG
- Sophie Cros, Director, Regulatory Affairs, Reimbursement and Health Economics EMEA, Abbott Vascular International BVBA
- Ameer Ally, Director Healthcare Economics & Reimbursement, Surgical Solutions Europe, Covidien UKI & Norden
- Alice Campanini, Device Development Department, Chiesi Farmaceutici S.p.A.
- Pat Baird, Product Design Owner, Baxter Healthcare
- Dr. Peter Havel, Senior Vice President, Global Head of Medical & Health Services (MHS), TÜV SÜD Product Service
- Peter Schroeer, Director Europe Quality Systems & Regulatory Affairs, Johnson & Johnson
- Dr. Gert Bos, Head of Regulatory and Clinical Affairs Healthcare, BSi Healthcare
- John Brennan, Director Regulatory and Technical Affairs Eucomed
- Philippe Auclair, Pharmacist, PhD Senior Director, Regulatory Strategy and Advocacy, Abbott Quality & Regulatory EMEA, Abbott Vascular International
More information and registration at http://medteceurope.com/index.php?page=home-en.