REGASK TAKES THE STAGE
Unboxing Live by Esko 2025
November 18–19, 2025 | Virtual Event
Meet our team
Join this session to see how RegASK’s AI-driven regulatory intelligence integrates seamlessly with Esko’s packaging solutions, simplifying compliance, boosting speed, and empowering teams to deliver accurate, compliant, and sustainable packaging more efficiently.
🎙 Speaking Session
Rohit Gulati, Head of Product, RegASK
🕒 5:50 PM – 6:10 PM | Tuesday, 18 November 2025
Topic: “Navigating Regulatory Complexity with Confidence: Esko & RegASK Integrated”
Rohit Gulati
Head of Product
Unboxing Live by Esko 2025
Unboxing Live is a premier global virtual event that brings together innovators and leaders shaping the future of packaging and labeling, from brand owners and converters to regulatory professionals and technology pioneers. Over two inspiring half days, participants will explore the latest trends, insights, and solutions driving compliance, sustainability, and quality in packaging operations worldwide.
Key Themes Include:
- Exclusive market insights to stay ahead of emerging trends
- Real-world customer success stories and interactive panels with industry experts
- New Esko innovations to optimize compliance and sustainability in packaging
- Strategies for artwork management, labeling, and production efficiency
Venue & Schedule:
📍 Virtual Event (Global Access)
🗓 November 18–19, 2025
🕒 3:00 PM – 6:30 PM CET | 9:00 AM – 12:30 PM ET
Resources
Navigating a Potential U.S. Government Shutdown: Implic…
As legislators in Washington, DC, face a critical March 14th deadline to finalize federal spending, the possibility of a U.S. government shu…
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RegASK Featured in Gartner’s Market Guide for Regulat…
We’re thrilled to share that RegASK has been included in Gartner’s Market Guide for Regulatory Intelligence Solutions! This recognition …
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The 2025 State of Regulatory Affairs and Compliance Rep…
Is your organization prepared for 2025’s regulatory complexities? The regulatory landscape in 2025 is more complex than ever, with new adv…
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ANSM (France) Clarifies CE Mark Exemption Process for M…
On January 27, 2025, the National Security Agency of Medicines and Health Products (ANSM) in France issued a key update regarding the proces…
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US FDA Announces Draft Guidance on AI Use in Regulatory…
On January 6, 2025, the U.S. Food and Drug Administration (FDA) announced the release of a draft guidance titled “Considerations for the U…
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US FDA Announces Public Meeting on Paediatric Legislati…
The Food and Drug Administration (FDA) has scheduled a public meeting titled “Interested Parties Meeting: Implementation of the Best Pharm…
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FDA (USA) Establishes New Center for Real-World Evidenc…
On December 12, 2024, the U.S. Food and Drug Administration (FDA) announced the creation of the Center for Real-World Evidence and Innovatio…
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Portuguese Industry Opposes U.S. Proposal for Cancer Wa…
The United States Health Authority is considering the introduction of mandatory cancer warning labels on alcoholic beverages, a measure simi…
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