Improve Pharmaceutical Packaging Throughput With Serialization

Serialization has helped pharmaceutical packaging lines meet compliance requirements, but it has also introduced operational challenges for many manufacturers and CMOs. Codes that fail to meet grading requirements, cameras that reject acceptable packs, exceptions that stop the line while operators identify the cause and rework loops that consume production capacity all contribute to lost throughput. This webinar explores practical strategies to identify serialization-related bottlenecks, reduce downtime and improve packaging line performance.

With capacity, staffing and profit margins under pressure, maintaining compliance while improving operational efficiency is increasingly important. Key performance measures include uptime, first-pass yield, exception resolution time and how quickly the line returns to normal production after a stop.

The featured panelists will examine common bottlenecks on serialized packaging lines and practical steps manufacturers can take to address them. The speakers will discuss the root causes of stoppages and rework, from device-level printing and inspection quality to line setup, exception handling and site-level serialization data management. Examples involving new line startups, technology transfers and CDMO client onboarding will illustrate how these principles apply to both existing and new packaging lines.

Attendees will gain insights into methods for diagnosing production losses, evaluating serialization performance and using integrated hardware, software and line data to support operational improvement while maintaining compliance.

Register for this webinar to learn how to reduce pharmaceutical packaging downtime, minimize rework and improve throughput on serialized production lines.