Dutch Clinical Research Foundation (DCRF) Congress 2018

De Reehorst Hotel
Bennekomseweg 24
Ede, Netherlands

The topics for the Dutch Clinical Research Foundation (DCRF) Congress 2018 were focused on clinical trials and research and the regulatory aspects of both. Cristiana Spontoni was a keynote speaker for this event. Her presentation focused on the Clinical Trials Regulation (CTR), the Medical Devices Regulation (MDR), and the General Data Protection Regulation (GDPR) and the impact of these new EU regulations on the EU clinical regulatory landscape.

Other topics included:

  • The transfer of the European Medicines Agency (EMA) to Amsterdam and the implications for clinical medicine and device research, presented by Maurice Galla, Coordinator of EU Policies, Minister VWS; and
  • The publication of clinical research results and the associated risk of bias in scientific literature, presented by Dr. Annelieke Roest & Dr. Sander van den Bogert.

Post-speech interview with Cristiana can be found here:

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