KCRI
Lidia Kabat is a Chief Safety Officer at KCRI since August 2016. Lidia also works as a Clinical Trial Senior Safety Specialist, responsible for safety monitoring in clinical trials including adverse events management, safety management plans, and communication with various stakeholders. Previously, Lidia held roles in pharmacovigilance, quality assurance, and completed internships in diagnostics laboratories. Lidia has a Master's degree in laboratory diagnostics and has completed post-graduate studies in Quality Manager.
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KCRI
KCRI is a provider of clinical research services for medical device manufacturers. We cover broad therapeutic areas, including but not limited to cardiovascular, orthopedics, general surgery, ophthalmology, pulmonary disease, and ob-gyn. We are also happy and excited to investigate new devices: mHealth / eHealth / algorithms/sensors/apps. With extensive therapeutic, scientific, and imaging expertise, we help health sciences customers achieve ambitious goals in a demanding regulatory environment. Proven regulatory knowledge in Europe, a team of dedicated PM and CRAs, professional data management and statistical services, Core Laboratories, and operations of Data Monitoring Committees - this is KCRI. Are you seeking an experienced CRO with a research perspective and medical device experience? Contact us at learnmore@kcri.org - we will help.