Pharmaceutical & Medical Device companies are facing many compliance, regulatory & transparency changes with stringent requirements having to be met in short time-frames.
Recently the European Union has approved new and important reforms on data protection and in six months’ time the first EFPIA disclosure report will be required.
In December 2015 the MedTech association published the latest update on the Code of Ethical Business Practice.

During this seminar we will endeavor to answer the following questions and provide you with pragmatic solutions:
• What are the implications of data protection and transparency implications?
• What are the important changes compared to the previous regulations?
• How to deal with cross border transfers of value?
• How to handle the consent?
• How to comply with global requirements and enforce local ones?


Barcelona: 1 March 2016
Madrid: 3 March 2016


Barcelona: Carrer de les Escoles Pies, 102, 08017 Barcelona
Madrid: Calle de Serrano, 116, 28006 Madrid


9:00 – 9:25
9:25 – 9:30
9:30 – 10:00
10:00 – 10:15
10:15 – 10:25
10:25 – 10:45
10:45 – 11:15
11:15 – 11:45
11:45 – 12:00
12:00 – 14:00

Welcome coffee
EU Data Protection Reform: First Approach
Consent & Claims Management in the EU: First Feedback
Q&A Session
Coffee break
How to Manage Transparency at Local and Global levels
EU Data Protection Reform: how to be ready – DPO role
Q&A Session
Tapas & B2B Meetings


Laurent Clerc


General Manager
Compliance & Transparency Expert

Miguel Geijo

Rousaud Costas Duran

Corporate & Compliance Partner Head of IT & Data Protection

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