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in Pharma Packaging

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Your Trusted Partner in Packaging

Learn About Our Vision for the Future And Grow with Us.

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Special Varnish Printing: A Smart Layer of Safety for Pharma Packs

In pharma packaging, even a clear coating can carry the critical responsibility of protection, compliance, and security. Special varnish printing — a transparent, precision-engineered layer — plays a crucial role in safeguarding medicine packs from physical wear, counterfeiting, and regulatory risks.

Beyond aesthetics, varnish protects printed data, deters tampering, and supports migration-safe compliance. As regulatory scrutiny increases, this silent layer is fast becoming a standard in high-performance pharma packaging.

What Is Special Varnish Printing in Pharma?

Varnish printing involves applying a thin, transparent layer over printed pharmaceutical packaging materials such as aluminum foil. In pharma, varnish serves both functional and protective purposes.

Types Commonly Used:

1. Gloss or matte finish:

Enhances visual quality and tactile experience

2. Security varnish:

Reacts under UV light for covert authentication

3. Textured varnish:

Distorts or cracks when tampered with

4. Migration-safe varnish:

Prevents leaching into drug formulations

Regulatory Standards It Supports:

  • EU 10/2011 (food-contact materials, including pharma)
  • US FDA 21 CFR (indirect food additives)
  • BfR (Germany), ANMAT (Argentina)
These global standards ensure that varnish does not compromise drug safety or chemically interact with active pharmaceutical ingredients (APIs).

1. Print Durability Under Pressure:

Blister packs and foil lids endure constant handling, high-speed filling lines, and variable temperatures. Varnish protects essential elements — batch codes, expiry dates, brand info — from smudging or abrasion.

2. Tamper Detection:

Special varnishes distort, crack, or reveal signs of interference when packaging is opened or manipulated, offering visible cues of tampering.

3. Invisible Security Features:

UV-reactive varnishes or tactile patterns create covert markers that are difficult to counterfeit yet easy to verify with proper tools.

According to WHO, over 80% of counterfeit cases begin with visible packaging anomalies. Tamper-evident varnish plays a vital first-line defense.

Pharma exporters must meet migration safety and anti-counterfeit guidelines in regions like Europe, Latin America, and Russia–CIS.

Special varnish coatings support:

  • Chemical stability throughout shelf life
  • Resistance to high heat during sealing or sterilization
  • Inert behavior near medicines
  • Compatibility with serialization and clean-room protocols

Packaging Performance That Builds Patient Trust

1. Tactile Recognition:

Textured varnishes help visually impaired patients identify dosage zones or branding by touch.

2. Secure and Elegant Branding:

Gloss, matte, or soft-touch finishes elevate shelf appeal while adding complexity for counterfeiters.

3. Print Longevity:

Varnish extends the life of essential information — from dosage details to barcodes — ensuring legibility during storage, shipment, and distribution.

Advantages of Special Varnish Printing at a Glance

FeatureImpact on Pharma Packaging
Tamper detectionVisual cues for unauthorized access
Low migration complianceSafe for contact with medicine packs
Hidden security elementsHard to replicate, easy to verify
Print and code protectionPrevents smearing, scuffing, and fading
Premium look and feelEnhances patient confidence and brand credibility

As counterfeit risks grow and compliance demands evolve, varnish printing is poised for rapid innovation:

  • AI-integrated varnish for digital scan verification
  • Smart coatings embedded in serialization workflows
  • Wider use in injectables, biologics, and cold chain packaging

Quality Tip:
Always conduct real-world simulation tests under humidity and cold chain environments to validate varnish performance globally.

Though invisible to the eye, special varnish printing offers visible, measurable benefits. From safeguarding drug information to providing a line of defense against tampering and non-compliance, it is an indispensable tool in modern pharmaceutical packaging.

At Sanwariya Packaging, we specialize in low-migration, security-grade varnish coatings designed for real-world performance and international compliance. Whether you’re upgrading your product’s safety or targeting export-ready quality, our solutions offer unmatched protection and precision.

Ready to apply this smart layer of safety to your next pharma pack?
Let’s create compliant, secure, and brand-trusted packaging — together.

Special Varnish Printing in Pharma: Protection with Visual Appeal

Author

Jay Wadhwani

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The Science of Barrier Protection: Why Aluminum Foil Works

In hot and humid regions like Latin America, Asia, and Africa, medicines can lose up to 30% of their potency within weeks if not packaged correctly. This isn’t just a patient safety issue — it can lead to failed stability tests, regulatory delays, costly recalls, and damaged brand reputation.

That’s why aluminum barrier foil is more than just packaging. It is the pharmaceutical industry’s most reliable safeguard against moisture, oxygen, light, and contamination — all factors that can shorten a drug’s shelf life or compromise its effectiveness.

Barrier protection is a material’s ability to shield medicines from environmental threats. Without it, even well-formulated drugs can degrade. The key elements barrier foil protects against include:

  • Moisture: It can trigger chemical breakdown, microbial growth, or active ingredient loss.
  • Oxygen: It can cause oxidation, reducing the drug’s potency.
  • Light: UV and visible light can destabilize sensitive drugs like vitamins, hormones, and antibiotics.
  • Contaminants: Dust and airborne particles can compromise sterility and safety.

These risks are magnified in countries classified as ICH Climatic Zones III and IV (hot and humid regions) under global stability guidelines. The International Council for Harmonisation (ICH) sets strict testing standards for medicines in these zones. Meeting these standards often requires high-performance aluminum barrier foil to ensure products stay stable and pass regulatory reviews.

Aluminum foil outperforms plastics like PVC or PVDC in nearly every key metric, providing unmatched barrier protection and regulatory reliability.

PropertyAluminum FoilPVC/PVDC Film
Moisture BarrierExcellent (WVTR < 0.01)Moderate (WVTR ~0.2–0.5)
Oxygen BarrierExcellentLow
Light Barrier100% ProtectionPartial
Chemical InertnessNon-reactiveMay leach under stress
RecyclabilityHighLow

Because it is non-reactive and chemically stable, aluminum is ideal for protecting moisture-sensitive, pH-sensitive, and light-sensitive drugs, ensuring they remain safe and effective until the end of their shelf life.

Where Barrier Foil Makes the Most Impact

  • Alu-Alu Blisters – Maximum barrier for highly sensitive tablets like antibiotics and blood pressure medicines.
  • PVC-Alu Blisters – A balanced, cost-effective solution for moderate protection needs.
  • Strip Packs – Ideal for powders, dispersible tablets, and single-dose products.
  • Sachets – Perfect for granules requiring airtight sealing.

The Business Case for Barrier Foil

1. Extended Shelf Life

Barrier foil helps products pass both real-time and accelerated stability tests, even in ICH Zone IV conditions, ensuring medicines remain effective until they reach patients worldwide.

2. Global Regulatory Compliance

Aluminum foil meets packaging standards from leading authorities, including:

  • US FDA
  • EMA (Europe)
  • TGA (Australia)
  • WHO Prequalification Programs

3. Using aluminum foil simplifies approvals and avoids packaging-related audit issues when entering multiple international markets.

4. Reduced Risk and Cost

By preventing degradation, foil packaging helps cut down on:

  • Stability failures
  • Recalls and returns
  • Customer complaints and brand damage

5. The result:

Lower quality costs and stronger market reputation.

To make sure your packaging performs as expected, every pharmaceutical company should:

  • Verify the foil’s moisture and oxygen transmission rates (WVTR and OTR).
  • Choose the right laminate structure (PET, PE, lacquer layers) for the product’s sensitivity.
  • Test sealing strength at the intended thickness and processing temperatures.
  • Conduct ICH-compliant stability studies under real-time and accelerated conditions.
  • Even a high-quality formulation can fail a stability study if the foil isn’t matched to the product or climate.

The pharmaceutical industry is moving toward solutions that balance performance, sustainability, and security, including:

  • Recyclable, ultra-thin aluminum foils that cut down on material waste.
  • Bio-based adhesives and coatings for greener laminate structures.
  • Smart foils with built-in tamper indicators, authentication features, and digital tracking via QR or NFC codes.
These advancements help manufacturers stay compliant while meeting growing environmental and anti-counterfeit demands.

In pharmaceuticals, packaging isn’t just a wrapper — it’s the final shield that protects your product, your brand, and ultimately, the patient. Aluminum barrier foil remains the most trusted and proven material for ensuring drug stability, safety, and compliance worldwide.

Whether your medicines face harsh climates, light sensitivity, or strict regulatory scrutiny, choosing the right barrier foil can protect your investment and reputation.

Let’s Talk Protection You Can Count On

At Sanwariya Packaging, we deliver science-backed, customized aluminum foil solutions that help pharmaceutical companies achieve stability, compliance, and market confidence.

Contact our technical team today for guidance or request a free barrier foil sample to see how we can protect what matters most — your product and your patients.

Barrier Foil in Pharma: How Aluminum Protects What Matters Most

Author

Jay Wadhwani

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Beyond the Surface: How Custom Foil Printing Builds Trust in Pharma

Patients don’t see your cleanrooms. They don’t read your batch release forms or regulatory filings. But they do see — and judge — your packaging. In that first glance, trust is either built… or broken.

In a global pharma market where brand credibility, safety, and compliance are under a microscope, packaging isn’t just functional — it’s emotional, strategic, and regulatory. And when it comes to pharmaceutical aluminum foil, custom printing isn’t a nice-to-have. It’s your frontline communicator.

The Silent Messenger: Why Patients Trust What They See

When a patient holds a strip of medicine, they’re holding a promise. But if that foil looks generic, poorly aligned, or faded — that promise feels weaker.

In a 2023 PharmaBrandWatch study, 35% of patients said they trust and recall medicines more when the foil is uniquely branded.

A custom-printed foil isn’t just packaging. It’s a signal of precision, quality, and professionalism. And in a world battling counterfeits, trust starts with what’s visible.

Five Branding Wins Only Custom Foils Can Deliver

Custom foil printing offers strategic advantages beyond aesthetics:

  • Faster Patient Recognition
    Color-coded SKUs and visible branding help patients and caregivers avoid medication mix-ups — especially important in chronic and pediatric care.
  • Higher Brand Recall
    Distinct logos, layouts, and foil finishes make your product memorable — vital in OTC markets where shelf appeal influences decisions.
  • Stronger Regulatory Clarity
    With region-specific printing, compliance details are built in — reducing relabeling, delays, and rejections during audits.
  • Unified Global Brand Identity
    Consistent foil design across countries reinforces your brand while meeting local regulations.
  • Enhanced Shelf Impact
    Even prescription meds compete for attention in retail environments. Well-designed foils command space and confidence.

Smart Design Features That Drive Compliance & Trust

FeatureStrategic Value
Multicolor PrintingDifferentiates SKUs and improves readability
Reverse-Side PrintingPrevents abrasion and ensures legibility
Microtext & QR CodesAdds anti-counterfeit security
Matte / Gloss FinishesMatches brand tone (clinical, pediatric, premium)
Custom Codes & TrackersEnables authentication and traceability


From Factory to Final Dose: Every Interaction Counts

Especially for chronic therapies, patients interact with packaging daily. If dosage info, expiry dates, or batch codes are unclear, confidence takes a hit.

Your foil is a communication channel. One that speaks clarity, safety, and legitimacy. From the production line to the pharmacy shelf, packaging must perform — not just protect.

Choosing a Foil Printing Partner: What Really Matters

Not all suppliers are created equal. Choose a partner who offers:

  • Multicolor high-resolution printing with cleanroom control
  • Anti-counterfeit features like hidden marks, microtext, and QR authentication
  • GMP compliance with full traceability
  • Regulatory experience in EU, USFDA, GCC, CIS
  • Batch-to-batch consistency with audit-ready documentation

Why Custom Foil Printing Isn’t Optional Anymore

  • Builds patient trust and strengthens brand equity
  • Reduces medication confusion and substitution risks
  • Supports country-specific pharma regulations
  • Reinforces authenticity and protects your reputation

Ready to Upgrade Your Foil — and Your First Impression?

Let’s design packaging that earns confidence — from regulators and patients alike.

👉 Request a Custom Foil Sample

At Sanwariya Packaging, we specialize in precision-engineered, regulation-ready aluminum foil printing with anti-counterfeit and brand-forward designs. Trusted by leading pharmaceutical companies across India, LATAM, Russia-CIS, and beyond.

How Custom Foil Printing Builds Trust in Pharma

Author

Jay Wadhwani

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Ensure seamless pharma exports to Latin America and Russia–CIS. Navigate serialization, anti-counterfeit mandates, and packaging laws with Sanwariya’s regulation-ready solutions.
Ensure seamless pharma exports to Latin America and Russia–CIS. Navigate serialization, anti-counterfeit mandates, and packaging laws with Sanwariya’s regulation-ready solutions.

In today’s global pharmaceutical landscape, packaging compliance isn’t a checkbox — it’s your entry pass. With Latin America and the Russia–CIS region emerging as high-potential markets, exporters must prepare for unique packaging regulations shaped by serialization mandates, multi-language labeling, anti-counterfeit features, and regional barcode standards.

This guide breaks down what it takes to confidently ship compliant pharmaceutical products to these dynamic regions — and how Sanwariya Packaging can support you at every step.

Understand the Regulatory Landscape

1. Latin America

Composed of key pharma markets like Brazil, Argentina, and Colombia, the region is regulated by national authorities such as:

  • ANVISA (Brazil)
  • ANMAT (Argentina)
  • INVIMA (Colombia)

2. Russia–CIS

Led by Roszdravnadzor (Russia) and governed under the Eurasian Economic Union (EAEU), these countries follow regionally aligned packaging and serialization protocols.

Each market enforces distinct requirements — making localized packaging expertise essential.

Compliance Snapshot: Latin America vs Russia–CIS

Regulatory FactorLatin AmericaRussia–CIS
Labeling LanguageSpanish or Portuguese (country-specific)Russian + local EAEU language (where applicable)
SerializationMandatory in Brazil (GS1 standard)Mandatory via Chestny ZNAK, Russia’s national track & trace system
Anti-CounterfeitNot mandated, but advanced features are encouragedTamper-evident and serialized packaging is legally required
Barcode StandardsVary by country; Brazil uses GS1 DataMatrixMandatory DataMatrix, linked to government-regulated platforms
Regulatory OversightANVISA, ANMAT, INVIMA, etc.Roszdravnadzor, EAEU Technical Committees

Top Challenges for Exporters

  • Fragmented Standards –Latin America requires country-specific packaging and label formats. Uniform solutions often fall short.
  • Serialization Mismatch – Brazil uses GS1, while Russia mandates Chestny ZNAK — two very different systems.
  • Language Errors – Missing technical terms or poorly translated medical details can lead to customs rejections.
  • Barcode Placement Issues – A 2mm error in barcode position or font size can delay approvals or lead to regulatory penalties.

How to Ensure Region-Ready Compliance

1. Work with Regulatory-Focused Packaging Partners

Collaborate with suppliers like Sanwariya Packaging, who are fluent in region-specific laws and technical nuances.

2. Use Flexible, Multi-Market Designs

Opt for packaging templates built to accommodate different label languages, serialization formats, and anti-counterfeit elements.

3. Deploy Serialization-Ready Printing

Invest in GS1-compliant and Chestny ZNAK-ready print systems — including high-precision DataMatrix and tamper-evident features.

4. Test with Local Compliance Experts

Validate final packaging with local auditors or consultants before launch to prevent errors and costly delays.

From Hurdle to Opportunity: Make Compliance a Competitive Edge

“The real cost isn’t compliance — it’s non-compliance.”

Compliance is no longer a burden — it’s your brand advantage. With Sanwariya’s support, you gain:

  • Faster product approvals
  • Fewer returns or repackaging costs
  • Stronger regulatory trust
  • Export-readiness across multiple geographies

Pharmaceutical packaging compliance in Latin America and Russia–CIS demands precision, expertise, and proactive execution. With regulatory frameworks tightening across both regions, exporters can no longer afford to treat compliance as an afterthought.

At Sanwariya Packaging, we specialize in high-performance, regulation-ready aluminum foil solutions — tailored for the global pharma landscape. From multi-language labeling and GS1 serialization to Chestny ZNAK compliance and tamper-evident printing, we make sure your packaging meets every requirement the first time.

Exporting to Latin America or Russia–CIS?
Let Sanwariya Packaging ensure your compliance — and your confidence.

Contact us today for tailor-made foil packaging solutions that protect your product, reputation, and global reach.

 

Regulatory Readiness in Latin America & Russia-CIS: What Exporters Must Know

Author

Jay Wadhwani

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NC-Free Printing- A Safer, Greener Future for Pharma

In an industry governed by safety, precision, and regulatory rigor, pharmaceutical packaging must keep pace with evolving environmental standards and worker protection mandates. One critical area of change is ink formulation—specifically, the move away from nitrocellulose (NC) inks.

NC-free (Nitrocellulose-free) printing is no longer a niche trend—it is a strategic upgrade. With global compliance requirements tightening and sustainability becoming a core brand pillar, the shift to NC-free inks offers pharmaceutical companies a safe, compliant, and environmentally responsible solution.

What Are NC-Free Inks—and Why Do They Matter?

Traditionally, NC-based inks have been favored for their fast drying and vivid visual output.

However, these inks come with significant drawbacks:

  • High VOC Emissions: Contributing to indoor air pollution and regulatory non-compliance.
  • Flammability Risks: NC-based inks are highly flammable, posing operational and storage hazards.
  • Disposal Challenges: Waste disposal from NC inks often violates environmental regulations in key export markets.
By contrast, NC-free inks are engineered to meet the same print performance standards—while drastically improving safety, environmental impact, and compliance.

Why Leading Pharma Brands Are Switching

Pharmaceutical manufacturers and CMOs using NC-free foil systems have reported measurable improvements:

  • Reduced Fire Risk — Safer working environments due to the elimination of flammable NC components.
  • Better GMP/EHS Audit Outcomes — Lower VOC output improves audit readiness and compliance ratings.
  • Waste Management Simplified — NC-free systems ease the burden of hazardous waste treatment.
  • Enhanced Brand Reputation — Demonstrates environmental responsibility to regulators, partners, and consumers.

Case Insights:
A European generics manufacturer observed a 15% reduction in packaging-related safety incidents within six months of adopting NC-free foil printing.

Compliance-Focused Printing: A Must for QA Teams

For Quality Assurance and Compliance leaders, NC-free inks align with pharmaceutical best practices. Key elements include:

1. Validation Readiness

NC-free systems support standard cGMP foil printing workflows and undergo:

  • Adhesion testing
  • Color consistency benchmarking
  • Solvent and chemical resistance checks

2. Audit Documentation

Ensure your packaging partner supplies:

  • VOC emission reports
  • Ink formulation data & batch traceability
  • REACH, RoHS, and other regulatory certifications

Supplier Qualification Checklist

RequirementWhat to Look For
Certified NC-Free Ink UsageVerified with technical data sheets
Validated WorkflowDocumented QC, ink handling, waste policies
Pharma-Specific CustomizationFonts, readability, and barcode clarity

NC-free ink systems contribute significantly to pharmaceutical sustainability initiatives:

  • Lower Emissions: Significant reduction in VOCs contributes to cleaner air.
  • Smaller Carbon Footprint: More efficient manufacturing and disposal.
  • Compliance with ESG & SDGs: Supports ISO 14001 and corporate ESG reporting mandates.

These factors are increasingly important in regulatory approvals and contract manufacturing evaluations—especially in the EU, Latin America, and emerging markets adopting green policies.

Common Concerns About NC-Free Inks

ConcernReality with NC-Free Solutions
Drying SpeedModern systems support high-speed curing
Color PerformanceRich pigments ensure brand consistency
Initial Cost of ChangeoverROI through safety, compliance & efficiency

NC-free systems are no longer experimental—they are proven, validated, and scalable for commercial pharma operations.

Time to Rethink Ink

Switching to NC-free ink systems is not just an environmental upgrade—it’s a forward-looking compliance and safety strategy. Pharmaceutical companies that make the switch benefit from improved regulatory outcomes, enhanced workplace safety, and strong ESG positioning.

At Sanwariya Packaging, we offer end-to-end NC-free foil printing solutions tailored for pharmaceutical use. Our inks are:

  • cGMP-compliant
  • VOC-tested and certified
  • Backed by stability data, regulatory documentation, and print durability reports

Let us help you build packaging that’s safer for your teams, smarter for your audits, and greener for your brand.

📞 Ready to go NC-free?

Contact Sanwariya Packaging today to explore customized foil printing solutions aligned with your compliance and sustainability goals.

NC-Free Printing: A Safer, Greener Future for Pharma

Author

Jay Wadhwani

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How Printing Technology Impacts Pharma Packaging Efficiency

In pharmaceutical packaging, the quality of print is directly tied to patient safety and regulatory success. Whether it’s batch numbers, expiry dates, or serialized codes—accuracy, legibility, and durability are non-negotiable. As the industry prioritizes compliance, efficiency, and traceability, choosing the right printing method becomes a strategic decision.

This article compares gravure and flexo printing technologies in the context of pharmaceutical packaging, helping quality assurance teams and decision-makers understand which approach best supports regulatory alignment, operational efficiency, and packaging performance.

1. Why Printing Matters in Pharma Packaging

Printing isn’t just visual—it’s functional. In regulated markets, it ensures:

  • Traceability: Serialization codes and data matrix elements meet DSCSA, EU FMD, and other global standards.
  • Patient Safety: Clear dosage instructions, expiry dates, and warning texts help prevent medication errors.
  • Audit Preparedness: High print fidelity ensures packaging withstands scrutiny from inspectors and regulators.
Packaging errors caused by smudged ink, unreadable text, or inconsistent colors can trigger batch recalls, compliance flags, or market rejections—resulting in financial and reputational loss.

2. Gravure vs. Flexo

FeatureGravure PrintingFlexo Printing
Print PrecisionSuperior for fine details, ideal for small fonts & barcodesAdequate for bold text and graphics
Setup & SpeedLonger setup, but highly efficient for large volumesQuick setup, efficient for short runs
Color AccuracyConsistent over long print runsMay show drift over extended runs
Cost StructureHigher upfront investmentLower initial costs, flexible for smaller batches
Material CompatibilityExcellent with aluminum foil and multi-layer laminatesPerforms well on paper and flexible film
Best Use in PharmaIdeal for high-security primary packagingSuitable for labels and secondary packaging

3. Gravure: The Gold Standard in Pharma Packaging

Gravure printing is engineered for high-volume, high-precision pharmaceutical applications, especially for aluminum foil substrates used in blister and strip packaging.

Key Benefits:

  • Microtext & Serialization: Maintains sharpness even at high speeds for compliant traceability codes.
  • Security Features: Supports reverse-side printing, invisible inks, and tamper-evident designs to prevent counterfeiting.
  • Durability: Ink adhesion on foil resists heat, light, and moisture—essential for global distribution.

Advanced Gravure Capabilities at Sanwariya Packaging:

At Sanwariya, we take gravure a step further with:

  • Multicolor Specialized Printing: Delivering exceptional color depth and consistency for brand-critical pharma packs.
  • Front-Back Online Printing: Simultaneous double-sided printing enhances efficiency and counterfeit resistance.
  • Special Varnish Printing: Provides extra abrasion resistance and visual appeal with medical-grade coatings.
  • NC-Free (Nitrocellulose-Free) Inks: Sustainable, low-VOC formulations that align with stringent international regulations.
Manufacturers using Sanwariya gravure solutions have reported 30–35% fewer print-related deviations, reduced label mix-ups, and improved scanner-read rates during serialization audits.

4. When Flexo Works Best

While gravure dominates high-security pharma packaging, flexo offers advantages in specific scenarios:

  • Short Runs or Customization: Ideal for pilot batches, marketing samples, or region-specific products.
  • Secondary Packaging: Works well on carton boxes, labels, and pouches where ultra-fine detail is not critical.
  • Speed-to-Market: Quick setup supports rapid design iterations and faster go-to-market timelines.
For pharma companies balancing cost and flexibility, flexo is a practical solution for non-critical packaging layers.

Invest in the Right Print Technology for Long-Term Gains

In the race to stay compliant, efficient, and secure, printing technology is a core enabler of pharmaceutical packaging success.

  • Gravure printing, with its unmatched precision and ability to integrate multilayered security, is ideal for primary pharma packaging.
  • Flexo printing, on the other hand, supports agility and cost efficiency in secondary layers or short-run needs.

Partner with Sanwariya Packaging for Compliance-Driven Innovation

At Sanwariya Packaging, we specialize in gravure-printed aluminum foils tailored for pharmaceutical applications. Our solutions meet the highest global standards for clarity, compliance, and performance.

We help brands:

  • Enhance packaging precision
  • Strengthen serialization integrity
  • Combat counterfeiting with advanced print features
  • Improve sustainability with NC-free, eco-conscious inks

Let’s Raise Your Print Quality and Lower Your Compliance Risk

If your team is evaluating printing technologies, speak with experts who understand the regulatory, operational, and security needs of the global pharma sector.

Let’s talk about how we can future-proof your packaging with the right print solution.

How Printing Technology Impacts Pharma Packaging Efficiency

Author

Jay Wadhwani

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