We are pleased to announce that Laura Castro joined the Qserve Group, where she is part of the Qserve CRO team and works as a Clinical Project Manager.
Laura will be responsible for leading the planning, setup, and execution of clinical investigations for medical devices and is based in the Netherlands. She works in close collaboration with the sponsor to develop the required documentation and obtain ethics approval and competent authority approval as well as manage the study from beginning to end.
Laura: “Working along with experts in the field of MedTech Regulatory, Clinical and Quality Compliance is one the greatest things of Qserve Group”
There’s a personal profile
available on this website where Laura explains more about her experience and core competencies.About Qserve Group
Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO and quality services.
Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing in medical devices. Check our current vacancies.