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Thursday, February 7 • 09:15 - 10:15
#S0405: Reducing Cost and Improving Quality of Clinical Trials

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Component Type: Session

Discover three questions to ask before you innovate to reduce cost and improve quality of clinical trials from lessons learned.

Chair

Clara Heering, MS, MSc

Speaker

Evolution of RBM - Risk-Based Quality Management
Artem Andrianov, PhD, MBA

Implementing a Scalable Risk-Based Monitoring Strategy
Richard Davies

How to drive forward clinical development between Japan and EU?
Hideyuki Kondo, MBA

An Integrated Artificial Intelligence Platform for Clinical Study Management
Manfred Koehler, DrSc



Speakers
avatar for Artem Andrianov

Artem Andrianov

CEO, Cyntegrity Germany GmbH
"Artem Andrianov graduated with degrees in software engineering, and MBA. After graduation, he defended a PhD with the focus on mathematical modeling. Artem started his career at CareFusion, and after three years shifted to the position of Development Manager with a focus on Data... Read More →
avatar for Richard Davies

Richard Davies

Vice President, Solution Expert, CluePoints
Richard Davies joined CluePoints in September 2018 and is based in the UK. As VP, Solution Expert his role is to support organizations’ adopting CluePoints solutions from a technical, functional and business process perspective, particularly as they execute their vendor selection... Read More →
CH

Clara Heering

Enterprise JJCO lead for Capacity & Alliance Management, Johnson & Johnson
Clara Heering is lead for Capacity and Alliance management at Johnson & Johnson Clinical Operations. Clara began her career as Research Fellow at Harvard Medical School, then joined Pfizer in Clinical Research & Development, where she served in roles of increasing responsibility for... Read More →
MK

Manfred Koehler

CEO, Koehler eClinical GmbH
CEO and Founder KOEHLER eClinical GmbH in Freiburg, Germany.
avatar for Hideyuki Kondo

Hideyuki Kondo

Deputy Director, Office of International Program, Pharmaceuticals and Medical Devices Agency (PMDA)
Hideyuki Kondo experienced, for more than 10 years of carrier in Ministry of Health, Labour and Welfare, Japan, several positions in the field of pharmaceutical and medical device regulations, including those related to pre-market review policies, GMP/QMS inspections, post-market... Read More →


Thursday February 7, 2019 09:15 - 10:15
F1 Austria Center Vienna Bruno-Kreisky-Platz 1 1220 Vienna Austria
  • Featured Topics Clinical Development
  • Tags Session