Cross-Contamination Prevention Online Event

Event Details
Director of Process Technology
FPC Life Sciences
EMEA Training Manager & Critical Environments Specialist
DuPont de Nemours
Senior Technical Service Manager
STERIS Corporation
CEO
Packaging Technologies & Inspection (PTI)
Senior Subject Matter Expert-Aseptic Fill Finish/Freeze Drying
WuXi Biologics

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)

  • Keys to Developing a Multi-Site Contamination Control Strategy
  • Utilizing your Cleaning and Disinfection Program to Prevent Cross Contamination
  • Proactively Utilizing Continuous Improvement in Your Contamination Control Program

  • Reasons Why Cleanroom Garments Must Be Worn in Cleanrooms
  • Assessing the Performance Requirements of Cleanroom Garments
  • Different Garments for Different Cleanrooms

  • How Clean Is Clean And How Dry Is Dry?
  • Design For Cleanability. How Far Should We Go?
  • Limitations Of Riboflavin For Sprayball Coverage Testing. Can We Do Better?

  • Refill your drink
  • Grab a snack
  • Importance of Contamination Control in Pharmaceutical Manufacturing
  • Risks Associated With Contamination (Product Safety, Regulatory Compliance, Batch Failures)
  • Overview of Decontamination Methods in the Industry (Key Technologies)
  • Benefits of Implementing a Rapid Decontamination Station
  • Introduction to the Concept of a Rapid Decontamination Station (RDS) and Its Role in Improving Control Measures
  • Case Studies & Real-World Applications

  • Explore The Core Components Of CCS And How Each Relates To Container Closure Integrity.
  • Highlight CCI As The Final Barrier To Contamination, Ensuring Sterility By Extending Contamination Control Beyond The Manufacturing Environment.
  • Map The End-To-End Process, Illustrating How CCI Integrates With CCS To Deliver Safe And Sterile Pharmaceutical Products While Meeting Regulatory And Quality Standards.

  • FULL ACCESS
    Early Bird in February
    245
  • Full online access
  • Post-event documentation
  • Certificate of attendance
  • Cross-Contamination Prevention Online Event
    Name
    Name
    First
    Last
    Agree
    Leave a Comment

    Event Details