About

Mrs. Kfir has been involved in the Clinical Studies field for over a decade and has experience in all possible facets of clinical trial activities and procedures. With extensive knowledge in both medical device and pharmaceutical trials, she has been involved and managed many trails to successful FDA, CE and MHO approvals.

Additional Background

Mrs. Kfir has a vast portfolio of services from the initial stages of planning and outlining clinical studies, preparing all the required submission documents, establishing collaborations, clinical study site initiation, recruitment and monitoring of study subjects and operations.
Today, as part of the liberDi team, Mrs. Kfir provides clinical trial management and
monitoring services.