Specializes in comprehensive assistance to clients from the Life Sciences industry. She advises in the ongoing business activity on medicines, medical devices and food supplements market, at every stage of the product lifecycle – from clinical trials, through placing on the market, contracts, advertising, to actions associated with the products’ safety, incl. internal investigations and product liability disputes. She represents clients before competent authorities and state courts. 

Graduated from University of Poitiers (Master in French and European Business Law, M2) and British Law Centre (two-year Diploma Course in English and European Union Law). 

Member of the Committee of Appeals for Benefits from the Clinical Trials Compensation Fund by the Patients’ Rights Ombudsman.   

Expert in CASE – Center for Social and Economic Research on legal aspects of the projects concerning sustainable development. 

Leader of the project „Small Patients in clinical trials” („Mali Pacjenci w badaniach klinicznych”) in K.I.D.S. Foundation. 

Recommended by Legal500 in the Life Sciences & Healthcare category since 2022.