"B.Sc. in Applied Chemistry Analytical Method Validation for FDA Compliance “The Center for Professional Advancement, Amsterdam Netherlands. ISO-13485 training by PUM senior expert of Netherlands. Participation (Method of Analysis Development) in the 5th Scientific Congress of the Association of the Colleges of Pharmacy in the Arab World & the 2nd International Conference of the Faculty of Pharmacy “New Millennium, New Horizons in Pharmaceutical Sciences” 10 years of experience in analysis Development and validation Section head research and development department / Dar Al-Dawa. 7 years of experience in Quality Control Manage r (QC). Good experience on (GMP) Good Manufacturing Practice. Good experience on the following laboratory instrument (operation , and calibration) , HPLC, GC , UV/VIS spectroscopy , IR , melting point , thin layer chromatography , atomic absorption dissolution test , disintegration , hardness friability test. Good experience on stability testing of drug product , and method of analysis development and validation according to ICH guideline."

Quality Control, GMP, Pharmaceutical analysis