Femke Valkenburg

Clinical Study Design Expert
Femke Valkenburg, MSc.
Clinical Evaluation Consultant

 
Femke has joined the Qserve Clinical Affairs team, supporting customers with Clinical strategy development, Clinical Investigation and Clinical evaluation. Femke has key experience with high-risk active (implantable) devices in the field of Neurology and Radiology. 

Prior to Qserve, Femke performed her PhD studies in Biomedical Sciences at the University of Antwerp, Belgium, in the field of Neurosciences, and more specifically, Neurodegenerative diseases. Here, she became interested in the ethical considerations concerning (pre)clinical testing and guidelines and regulations regarding the development of medical devices. In addition, she gained experience with EU regulations concerning preclinical testing. 

Femke holds an MSc in Biomedical Sciences: Neurosciences, and is currently in the final stage of finishing her PhD. She has a broad experience in (pre)clinical research and medical writing and approaches this in a practical, logical way, always keeping in mind the customer’s needs.

Femke about working at Qserve:
“With the new MDR and the MEDDEV rev.4, the quality of your clinical data is rapidly becoming more important. I particularly enjoy the challenge to support companies in their trajectory to successful market access, while maintaining the high-quality standard that Qserve stands for. From initial (pre)clinical studies, until PMCF planning, analysis and interpretation: we can support you in a practical and efficient manner.”
 
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