Medical Device Labeling Best Practice for 2025: The Global Design Master
Tuesday, January 21 | 3:00 PM ET US
Program:
Join us for a forward-thinking webinar tailored for labeling and regulatory professionals in the medical device and pharmaceutical industries. Gain key insights into the latest strategies, tools, and best practices needed to elevate your labeling processes, ensure compliance, enhance speed-to-market, and improve cross-functional visibility.
This session will feature a special interview with Pete Jenny the Vice President of I/T, Global Operations, and Supply Chain at Cardinal Health, a leading medical device company, sharing their experience in leveraging new technologies to optimize labeling processes. Attendees will hear firsthand how Cardinal Health is adopting innovative solutions to streamline label management, improve approval workflows, and maintain regulatory compliance on a global scale.
Advanced Labeling Technologies for 2025 and Beyond: Explore the newest developments in labeling software and how to implement adaptive technologies that meet the diverse needs of global markets. Learn how cloud-based platforms, AI, and data analytics are being used to drive accuracy, consistency, and visibility across all labels.
Creating a Global Design Master: Discover best practices for implementing a centralized "Global Design Master" strategy. By consolidating label content and design into a single framework, large enterprises can reduce duplication, cut down on manual updates, and ensure all labels meet global and regional standards.
Streamlining Compliance and Approval Processes: Compliance requirements are always evolving. This webinar will offer strategies for optimizing review and approval workflows to speed up regulatory clearance while safeguarding accuracy and quality.
Achieving Visibility Across the Product Lifecycle: Visibility is critical for keeping labels up-to-date, on-brand and compliant at every stage. We’ll discuss methods for increasing traceability, so teams can monitor each label revision and proactively address potential compliance risks.
Learning Objectives:
- Insights from Cardinal Health’s leadership on using technology to enhance labeling processes
- Best practices for implementing a global labeling design master
- Techniques to speed up approval flows and gain faster market access
- Strategies to enhance label visibility and lifecycle management
Don’t miss this unique opportunity to learn from industry experts and see how Cardinal Health is shaping the future of medical device labeling!
Presenter:
Pete Jenny
Pete is Vice President I/T, Global Operations and Supply Chain at Cardinal Health. He is responsible for supporting Distribution, Warehouse, Manufacturing and Supply Chain operations worldwide.
Currently he is driving the I/T digital transformation of both manufacturing and supply chain. Prior to join Cardinal Pete has held multiple leadership and system development positions with companies like Computer Science Corportation, Unisys, and General Dyanamics.
Pete has a BS in Applied Chemistry and a BS in Electrical Engineering from Valparaiso Indiana. He resides in New Albany Ohio with his wife and 5 kids.
Gurdip Singh
Gurdip is a deeply experienced leader and practitioner in life sciences industry transformation. Before joining Kallik as CEO, he held senior life sciences and healthcare industry leadership roles at CSC, then DXC Technology.
He enjoys being an executive hands-on leader, driving organizational transformation in heavily-regulated industries, where he has been actively delivering change for the last decade as a visionary, an advisor and practitioner in leadership, growth, transformation and complex program delivery.
Gurdip’s unique blend of business transformation, change management, and modern technology experience make him ideally placed to help regulated organizations drive greater consistency and integrity in critical global processes. He is driven in particular by a passion for people leadership and for growing talent.