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Xtalks, Online
2024-02-20
Many manufacturing companies within The Food and Drug Administration-regulated industry embracing Pharma 4.0 may encounter confusion and uncertainty when it comes to implementing warehouse automation and logistics within the facility. This webinar is specifically designed to discuss the implementation of warehousing and logistics, providing the attendees with the clarity they need to succeed in implementing dock-to-dock manufacturing.
Throughout this engaging session, industry experts will provide clear explanations of automated storage and retrieval systems (ASRSs), automated guided vehicles (AGVs) and their interfaces with automated warehousing software and production equipment. Attendees will be provided with a clear understanding of how these systems interface with each other and how traceability of products throughout the entire manufacturing site can be implemented. In addition, the key goals of automated warehousing and logistics and its fundamental concepts will be reviewed. Further, the essential principles of how these concepts impact quality, safety and compliance will be discussed.
Understanding the specific scenarios and circumstances to consider when designing and implementing automated logistics will allow organizations to make informed decisions when it comes to computer system and equipment design conceptualization, ultimately ensuring compliance.
As the pharmaceutical industry embarks on its industrial revolution through Pharma 4.0, staying ahead of the curve is crucial. Join this webinar to embrace the future of dock-to-dock manufacturing.
Keywords: Pharmaceutical Manufacturing, Pharmaceutical Supply Chain, Automation, Regulatory, Supply Chain/Logistics, Quality
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Organized by:
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Xtalks |
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Invited Speakers:
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Scott Council, Division Director – North Carolina, Performance Validation
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Deadline for Abstracts:
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2024-02-20
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Registration:
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Free Registration
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E-mail:
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tristan@xtalks.com
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