Program
| 08.30-09.00 | Registration and Coffee |
| 09.00-9.10 | Welcome and Introduction Yves Geysels, President ACRP.be |
| Moderator morning session: Dr. Josse Thomas | |
| 09.10-9.40 | Clinical Trials Regulation: Main Challenges and Changes Greet Musch, FAGG |
| 09.40-10.15 | The Medical Device Regulations Dario Pirovano, Regulatory Adviser, Eucomed |
| 10.15-11.00 | The Value of Integrity Frank Wells |
| 11.00-11.30 | Coffee |
| 11.30-11.55 | Parkinson Research from a patient perspective Dr Silvia Nezosi, UK |
| 11.55-12.20 | Quality and Informed Consent Procedures Hilde Maes, Oncology Research Center, GZA |
| 12.20-13.00 | Threads and opportunities of Clinical Research in 2015 Dr. Bernard De Bruyne, MD, Cardiovascular Center OLVZ Aalst |
| 13.00-14.00 | Lunch |
| Moderator afternoon session: Dr. Robert Lins | |
| 14.00-14.25 | Changing Role of CRA in Data Driven Trial Execution Oliver Boden |
| 14.25-14.50 | Patient participation in clinical trial development Elizabeth Vroom, NL |
| 14.50-15.40 | Panel discussion: How to adapt Clinical Trial Execution unique development needs in Biotech Annegret Van der Aa, Clinical Operations, Galapagos Ian Rentsch, Chair ACRP Deutschland e.V |
| 15.40-16.05 | Cathedral Challenges What happens after what comes next? Herman Konings, Trendwatcher |
| 16.05-16.20 | General Conclusion |
| 16.20 | Reception |