Jurgita Žuklijienė has extensive experience in regulatory affairs, having worked as a Regulatory Affairs Expert at Oy Medfiles Ltd, a Regulatory Affairs Specialist at UAB Medfiles, and a Regulatory Affairs Specialist at JSC Actiofarma. Jurgita is skilled in granting marketing authorization for medicinal products via national, DCP, and MRP procedures, as well as preparation and submission of registration dossiers and handling MAH transfers in eCTD program. Jurgita holds a Bachelor's degree in Physiotherapy from Lithuanian Sports University.
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