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Esther Daemen

Quality &Training Director – Data Protection manager, TRIUM Clinical Consulting

Esther Daemen is currently Quality & Training Director – Data Protection Manager at TRIUM Clinical Consulting and has over 27 years of working experience in the healthcare/pharma & device field.  She served many organizations in different research roles and as professional development director at ACRP global.

Esther gained a bachelor in nursing and earned project management, training and DPO certificates as well as and a master’s degree in Business. She is also a highly sought after presenter at professional conferences/universities and a writer of peer-reviewed articles for professional magazines like The Clinical Researcher.  Her work was rewarded by the KP Morgan OECT Summit 10Years Speaker Achievement Award in 2020, the Best trainer to watch 2010 Training Magazine award and by having her organization Kendle being listed as one of the top 125 training providers in the world in 2008.

About TRIUM Clinical Consulting:

TRIUM is an expert Contract Research Organization that offers a unique combination of global CRO services, staffing solutions, quality services, GDPR consultancy and risk-based approaches as well as training services.
It’s our mission to be a passionate, dedicated business partner with a focus on excellence to provide start‐to‐finish clinical trial activities tailored to the timing, budget and specific needs of the Sponsor.


The impact of the MDR and ISO 14155 update on Clinical Trials

Location Einstein C Room Start / end time 3:30 pm to 4:15 pm

The MDR becomes effective in May 2020 and an updated ISO 14155 standard is also expected soon. If you wonder what this means and how big the impact will be on your device related clinical trials, then join this session. A mix of theoretical background and real life examples will be shared and discussed, ensuring you a good head start towards compliance.