webinar

AI in Packaging Compliance: What’s Changing and Why It Matters

November 20, 2025
May 20, 2026 | 11:00 AM CEST
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Registered attendees get early access to ComplAi

Trusted by 5000+ Brands
BorosilAmulP&GHimalayaNiveaBesins HealthcaresEmcureCatalyst Pharma
BorosilAmulP&GHimalayaNiveaBesins HealthcaresEmcureCatalyst Pharma

What this session covers

In this session, you’ll see how AI checks packaging and labeling compliance across ingredient statements, allergen declarations, claims, and other mandatory label elements, tailored to EU and Middle East requirements.

We’ll walk through how it identifies inconsistencies, flags risks early, and helps packaging and regulatory teams stay aligned before artwork goes to print, especially when managing multiple markets and variations.

You’ll also get a first look at our upgraded compliance module, ComplAi, designed to support multi-market labeling requirements in one place.

If packaging compliance still feels like a bottleneck, this practical session will give you a clearer and faster way to approach it in 2026.

Dr. Sridhar Swaminathan

Speaker

Shivashankar Balakrishnan

CRO @ ManageArtworks

Why this can't wait

EU PPWR kicks in August 2026

Regulation (EU) 2025/40 introduces new mandatory labeling rules, harmonised sorting labels,material composition disclosures, and PFAS bans — across all packaging, pharma included. No exemptions for secondary packaging.

Deadline: 12 Aug 2026

Non-compliance is getting expensive

Mislabeled products face recalls, trade restrictions, and EPR penalty fees. With regulators converging across EU, GCC, and global markets, a single label error now has multi-market consequences.

Rising cost of failure

Competitors are moving faster

Teams already running automated compliance reviews are cutting artwork rework cycles and getting to market quicker. Manual cross-checking across EU, GCC, and other variants is no longer a competitive option.

Speed to market

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See the difference

The compliance review your team runs today vs. the one you'll see on May 20.

How most teams do it today
Allergen declarations
Hours of manual work
Manually compared across variants. One spreadsheet, multiple people, no single truth
Claims validation
Inconsistent outputs
Googled, cross-referenced, debated. EU and GCC requirements interpreted differently by different people.
Artwork vs. approved copy
High error risk
Printed side by side, reviewed by eye. Errors caught here if you're lucky, at print if you're not.
Missing mandatory statements
Costly late catches
Found at final review or not at all. Rework triggered, timeline slips.
Multi-market consistency
Always the bottleneck
Done last, when everyone is tired. Highest-risk check, least attention.

WHAT CHANGES

What you'll see live on May 20
Allergen declarations
Minutes, not hours
Flag inconsistencies across all variants in one go. No spreadsheet, no manual cross-checking
Claims validation
Consistent every time
Every claim & other regulatory texts instantly cross-checked against current EU and ME guidelines
Artwork vs. approved copy
Caught at artwork stage
Compare artworks digitally against approved copy and spot every discrepancy before it reaches print.
Missing mandatory statements
Fixed before it compounds
Catch missing, incomplete, or outdated label elements early, before they trigger rework.  
Multi-market consistency
No longer the bottleneck
Run EU and GCC compliance checks in parallel from the start, not sequentially.
Everything in the right column is what we'll walk through live.  
See it in action & decide what it means for your team
Register now – Save my spot

Who should attend

Regulatory Affairs

Quality Assurance

Packaging Managers

Artwork Coordinators

Compliance teams in

Food

Beverage

Cosmetics

Personal Care

Wellness

Pharma

Trusted by over 5000+ Brands