

This event will gather pharmaceutical professionals, researchers, and experts to discuss key issues related to cross-contamination and its impact on patient safety. Due to recent incidents of cross-contamination, we aim to share practical information and case studies to mitigate contamination risks.
𝗞𝗲𝘆 𝗧𝗮𝗸𝗲𝗮𝘄𝗮𝘆𝘀
• 𝘊𝘰𝘮𝘱𝘳𝘦𝘩𝘦𝘯𝘴𝘪𝘷𝘦 𝘍𝘳𝘢𝘮𝘦𝘸𝘰𝘳𝘬 𝘧𝘰𝘳 𝘊𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘊𝘰𝘯𝘵𝘳𝘰𝘭
• 𝘐𝘥𝘦𝘯𝘵𝘪𝘧𝘺𝘪𝘯𝘨 𝘢𝘯𝘥 𝘔𝘢𝘯𝘢𝘨𝘪𝘯𝘨 𝘊𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘙𝘪𝘴𝘬𝘴
• 𝘛𝘦𝘤𝘩𝘯𝘰𝘭𝘰𝘨𝘪𝘤𝘢𝘭 𝘐𝘯𝘯𝘰𝘷𝘢𝘵𝘪𝘰𝘯𝘴 𝘵𝘰 𝘗𝘳𝘦𝘷𝘦𝘯𝘵 𝘊𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯
• 𝘙𝘦𝘨𝘶𝘭𝘢𝘵𝘰𝘳𝘺 𝘜𝘱𝘥𝘢𝘵𝘦𝘴 𝘧𝘰𝘳 𝘊𝘰𝘮𝘱𝘭𝘪𝘢𝘯𝘤𝘦
• 𝘓𝘦𝘴𝘴𝘰𝘯𝘴 𝘧𝘳𝘰𝘮 𝘙𝘦𝘤𝘦𝘯𝘵 𝘊𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯 𝘐𝘯𝘤𝘪𝘥𝘦𝘯𝘵𝘴
• 𝘈𝘥𝘷𝘢𝘯𝘤𝘦𝘥 𝘙𝘪𝘴𝘬 𝘈𝘴𝘴𝘦𝘴𝘴𝘮𝘦𝘯𝘵 𝘢𝘯𝘥 𝘌𝘹𝘱𝘰𝘴𝘶𝘳𝘦 𝘓𝘪𝘮𝘪𝘵𝘴
• 𝘖𝘳𝘨𝘢𝘯𝘪𝘻𝘢𝘵𝘪𝘰𝘯𝘢𝘭 𝘚𝘵𝘳𝘢𝘵𝘦𝘨𝘪𝘦𝘴 𝘵𝘰 𝘔𝘪𝘯𝘪𝘮𝘪𝘻𝘦 𝘊𝘰𝘯𝘵𝘢𝘮𝘪𝘯𝘢𝘵𝘪𝘰𝘯
𝗪𝗵𝗼 𝗦𝗵𝗼𝘂𝗹𝗱 𝗝𝗼𝗶𝗻
• Quality Assurance (QA) Manager/Director
• Quality Control (QC) Manager/Director
• Regulatory Affairs Specialist/Manager
• Microbiologist
• Process Engineer
• Validation Engineer
• Manufacturing Manager/Director
• Facility Manager
• Sterility Assurance Specialist
• Cleanroom Operations Manager
• GMP Compliance Specialist
• Pharmaceutical Scientist
• Research & Development (R&D) Scientist/Manager
• Risk Assessment Specialist
• Contamination Control Specialist
• Technical Operations Manager
• Pharmaceutical Consultant
• Principal Investigator in Pharmaceutical Research
• Auditor (GMP, FDA, MHRA, etc.)
• Supply Chain and Logistics Manager (for contamination risk in packaging and transport)
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