Urszula Krawczyk Email & Phone Number

Warsaw, Mazowieckie, Poland

Scope of activities: - GMP audits (product audit, process audit, supplier audit),- registration dossier CTD format Module 3 Quality, Module 2 Overall Quality Summary,- Quality Assurance consulting,- expertise on quality dossier for the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products in Warsaw, Poland,

Chemical analysis, medicinal product dossier assessment.

since August 1995Director’s Plenipotentiary for Quality Assurance,Implementation of ISO/IEC 17025 Standard.2001 – 2002PanEuropean Regulatory Forum (PERF) for Central and Eastern European Countries (CADREAC),Co-Chairman of the GMP Inspections Group,Preparation for access and compliance of Polish pharmaceutical industry to the EU regulations.1998 – 2000Ad.

Department of Herbal Medicines and Plant Materials.1992-1995: European Pharmacopoeia, observer in the group of experts No.13.

Laboratory of Alcaloids and Cardiac Glycosides, Department of Chemical Analysis

Ph. D., Pharmacy, Phytochemistry

M.Pharm., Pharmacy