Halima Jomli
Regulatory Affairs Manager at Novartis
Based in Tunis, Tunisia
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Seniority
Manager
Department
Science
Location
Tunis
Industry
Pharmaceutical Manufacturing
Company size
83K
Contact information
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h•••••••@novartis.com
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Background
About Halima Jomli
Coordinate and prepare high quality submissions of regulatory dossiers according to local regulation and international guidelines -Follow up dossiers under evaluation, answer Health Aouthorities questions and prioritize critical dossiers -Regulatory maintenance activities: variations, renewals, safety updates-Active negociations with Health Authorities (commitments) to submit dossiers and to ensure the continuity of the supply -Follow up closely the regulatory national and international environment -Solve supply issues and supply blocks in collaboration with supply chain team -Ensure optimal launch preparations for new products in close collaboration with product management, local and global supply chain management and quality assurance -Review and approval of promotionnal material, promotionnal and non promotionnal activities -Artworks creation, modification and approval -Track and communicate regulatory relevant activities, commitments, approvals, deadlines and events -Maintain country specific information in relevant databases and archives -Monitor national changes and communicate them to local and global teams and management as appropriate
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