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Advancing OSD Manufacturing with Dynamic Automation

| 7:00 p.m.

The Tour features revolutionary, technical, and “internet of things” concepts applied to pharmaceutical processing applications. Manufacturing is redefined by linking equipment or product assets with the ever-critical virtual information.

  • Brian Egan

    Senior Architect, Process Architecture

    In his 20 years of experience, Brian has assisted pharmaceutical companies in the manufacturing and distribution of product through the design and implementation of compliant facilities throughout the world. He leverages his international design experience and exposure to multiple facility design platforms, to challenge current thinking about the design of OSD facilities and material handling philosophies. This experience blends design philosophies from aseptic and bioprocessing into OSD facilities to create an optimal solution for the client. Brian is responsible for the overall design management of multiple biopharmaceutical manufacturing and research and development facilities. 
    In his 20 years of experience, Brian has assisted pharmaceutical companies in the manufacturing and distribution of product through the design and implementation of compliant facilities throughout the world. He leverages his international design experience and exposure to multiple facility design platforms, to challenge current thinking about the design of OSD facilities and material handling philosophies. This experience blends design philosophies from aseptic and bioprocessing into OSD facilities to create an optimal solution for the client. Brian is responsible for the overall design management of multiple biopharmaceutical manufacturing and research and development facilities. 
  • Lonna Gordon

    Process Engineer

    Lonna has over eight years of experience in GMP manufacturing with a focus on OSD process system design, from concept through construction. She has a strong background in contained powder handling, powder transfer, equipment design and selection, and capacity analysis. Her projects have ranged from multi-story gravity-fed wet-granulation trains to compliance remediation for generics manufacturing. Lonna is co-chair of the ISPE OSD Community of Practice and recently published an article on continuous manufacturing in OSD in Pharmaceutical Engineering Magazine. 
    Lonna has over eight years of experience in GMP manufacturing with a focus on OSD process system design, from concept through construction. She has a strong background in contained powder handling, powder transfer, equipment design and selection, and capacity analysis. Her projects have ranged from multi-story gravity-fed wet-granulation trains to compliance remediation for generics manufacturing. Lonna is co-chair of the ISPE OSD Community of Practice and recently published an article on continuous manufacturing in OSD in Pharmaceutical Engineering Magazine. 
  • Sam Halaby

    Sr. Director, Global Strategy & Technology

    Sam has over 20 years of experience in programming, design, and qualification of biotechnology and pharmaceutical facilities ranging from clinical to full-scale production plants. He is world-renowned for his application of “manufacturing dynamics” to the design of pharmaceutical facilities, as well as for his collaboration with other industry experts in global compliance, containment philosophy, and continuous manufacturing. Sam’s proven approach is designed to drive process architecture through the clear definition of unit operations and material movement with the ultimate goal of leveraging analysis tools to optimize production. He is currently the co-chairman of the ISPE Containment Community of Practice. He has formerly been the chairman of the ISPE Manufacturing Subcommittee and a steering committee member for ISPE Sterile Products Processing Community of Practice.
    Sam has over 20 years of experience in programming, design, and qualification of biotechnology and pharmaceutical facilities ranging from clinical to full-scale production plants. He is world-renowned for his application of “manufacturing dynamics” to the design of pharmaceutical facilities, as well as for his collaboration with other industry experts in global compliance, containment philosophy, and continuous manufacturing. Sam’s proven approach is designed to drive process architecture through the clear definition of unit operations and material movement with the ultimate goal of leveraging analysis tools to optimize production. He is currently the co-chairman of the ISPE Containment Community of Practice. He has formerly been the chairman of the ISPE Manufacturing Subcommittee and a steering committee member for ISPE Sterile Products Processing Community of Practice.

Thank you for your interest in the IPS Technologies Tours at INTERPHEX 2019! 

Online registration for IPS Technologies Tours at INTERPHEX is now closed.

Should you have any questions, please contact our Senior Marketing Specialist and Event Coordinator, Amy Armstrong, at aarmstrong@ipsdb.com or 610-828-4090 ext. 1015.

Please visit us at booth #2132.

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