At Qserve CRO, we take pride in our team of highly skilled professionals who are committed to delivering high-quality clinical trial services. Today, we are delighted to introduce Bianca Lutters, our Head of the Clinical Department at Qserve, with over 17 years of experience in strategic and decision-making roles in the medical device and IVD field.
Since 2022, Bianca has become the go-to person for 360-degree clinical support. She has worked for different Notified Bodies and held director positions in industry, bringing valuable knowledge and experience to the CRO. She tailors client expectations individually and consistently provides practical solutions.
Working in a CRO can be very dynamic, with many different aspects requiring attention during clinical trials. With Bianca’s expertise and experience, we are able to manage possibilities, focus on realistic investments of time and resources, and remain compliant with specific requirements. With her unique knowledge and hands-on experience, the CRO can offer services ranging from the strategic design of a study to finalizing reports for submission to the Notified Body, and everything in between. You can rely on Qserve CRO at every stage.
Based in the Netherlands, Bianca is the go-to person for our pre- and post-market studies on medical devices and IVDs. She is also a certified lead auditor and trainer for ISO 14155, ISO 13485, and MDR 2017/745.
Partner with Qserve CRO for your clinical trial. If you are looking for a reliable partner to conduct your study efficiently, ensure compliance, and avoid unnecessary shortcuts, Bianca and the Qserve CRO team are here to make sure your study runs smoothly and stays within budget. Contact us today!