Qserve is pleased to welcome 3 new colleagues:
Tran brings to Qserve more than 15 years of experience in Quality Management Systems Development and Process Improvement, Regulatory Compliance, and Regulatory Intelligence, as well as Internal and External Inspection/Audit Readiness activities. Her practical knowledge can be applied in Quality Management Systems, as well as EU MDR, and the Medical Device Directive. We are happy to welcome her as a member of our global team in the USA.
Ellen van Kleef
Ellen joined Qserve to further strengthen our clinical team and our broader global with a her wealth of knowledge across all aspects of clinical affairs. Ellen brings a lot of extensive experience in CRO related work, as well as project management with both medical devices and drugs. Additionally, she will support her colleagues in writing clinical evaluations, clinical protocols, and investigative brochures. We are thrilled to have her on our team. (view LinkedIn profile
With an focus in biostatistics and extensive experience in quality, regulatory, and clinical matters, Leonard brings a wealth of experience to our global team and significantly strengthens our competence in IVD products. We are thrilled to have Leonard join our US team! (view LinkedIn profile)