Summary: • + 25 years of expertise in supervising planning, carrying out, evaluation and reporting of Clinical Trials (Phase I –Phase IV drug trials, NIS, CE Certification trials of Medical Devices) of mostly all indications. • To get rid of redundancies and implausible or missing data in Clinical Trials Dr. Werdier invented, developed and patented ars® the first RDE/EDC system in Europe. System development has always been driven by optimization of self-evidence and user comfort of the system. • These roots led to the development of actually used modular tools to easily setup a system for clinical trials or set up a PMCF System for Medical Devices, where all parties of the project (patients, investigators, sponsor etc.) are included in the system. • These systems helped enormously saving time and money for Clinical Trials. All activities of Dr. Werdier and his staff comply with FDA/EMA, ICH/GCP and MDR requirements and SOPs of SAM GmbH.• Experience as Statistical/Medical Expert. Successful external trouble-shooter in several cases of emergency in clinical trials.• Strong analytic power as well as powerful creativity to analyse, to solve and to avoid existing problems causing trouble.• Looking forward to carrying out new interesting duties, responsibilities and projects.• Living in a +300 years old farmhouse near Aachen in Belgium• Giving animals in misery a new home• Sports: golf, tennis, hand gun & revolver shooting, boxing & fitness training