Omnia Moghazi
Head of Pharmacovigilance Department at Adwia Pharmaceuticals
Based in Cairo, Egypt
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Seniority
Director
Department
Science
Location
Cairo
Industry
Pharmaceutical Manufacturing
Company size
666
Contact information
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o•••••••@adwia.com
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Background
About Omnia Moghazi
Pharmacovigilance Manager with 8 years of experience as a drug safety professional, specializing in pharmacovigilance. Extensive background as a QPPV-Deputy, QPPV, and Pharmacovigilance Section Head within the pharmaceuticals industry. Commenced career with 13 years of experience in various community pharmacies. Also served as a compliance role for a short-term assignment of 4 months, overseeing the development and implementation process of local procedures for Adwia's governing SOP across all departments. Proficient in data analysis, project management, audit operations, meeting deadlines, and navigating Pharmaceutical Company Master Files. Experienced in fostering communication with Key Opinion Leaders (KOLs). Strong support professional with a Bachelor of Pharmacy (B.Pharm.) degree, focused on Pharmacy from Misr International University.Key Achievements- Recognized as the best employee for 3 consecutive years in the role of QPPV- Successfully managed and led the pharmacovigilance team at ADWIA- Obtained approval for Adwia's Pharmacovigilance System for the first time since its establishment in 2012- Achieved over 90% approval rate for product risk management plans, with effective implementation strategies for each product- Received appreciation in the form of "thank you letters" for signal detection and notifications submitted to EDA- Conceptualized a mobile application idea for medical representatives to streamline reporting processes- Implemented eight Pharmacovigilance Units at Adwia- Ensured comprehensive pharmacovigilance training for all employees, including new hires, through collaboration with the Human Resources department- Implemented customized software for efficient management of adverse event reports- Significantly increased awareness and reporting of adverse events, resulting in a more than 300% rise in the number of reports from 2020 to 2024, which has been sustained in the following year.
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