Meridan

Our Services

Comprehensive pharmaceutical contract packaging capabilities spanning primary and secondary packaging, serialization, cold chain, clinical trials, and packaging engineering - all delivered from three FDA-registered US facilities.

OVERVIEW

Meridan provides end-to-end pharmaceutical contract packaging services designed to meet the complex requirements of today's global pharmaceutical and biotechnology companies. From high-speed blister and bottle packaging to temperature-controlled biologics handling and fully serialized supply chains, our integrated platform delivers the quality, compliance, and throughput that commercial and clinical programs demand.

Every service is delivered within a unified quality management system spanning our three US facilities, ensuring consistent processes, documentation, and regulatory compliance regardless of which site or combination of sites supports your program. Our team of packaging engineers, quality professionals, and project managers works as an extension of your organization, managing the operational complexity so you can focus on bringing therapies to patients.

CAPABILITIES

Full-Service Packaging Capabilities

Six core service areas working together as a single, integrated packaging platform.

Primary Packaging

High-speed blister packaging, bottle filling, and vial and syringe packaging across all major dosage forms. Our primary packaging lines handle PVC, PVDC, Aclar, and cold-form aluminum blisters alongside HDPE and card-dark bottle configurations. Every line is equipped with integrated vision inspection and 100% in-process weight verification to ensure dose accuracy and package integrity.

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Secondary Packaging

Cartoning, labeling, kitting, overwrapping, and case packing with full multi-language capabilities and patient information leaflet insertion. Our secondary lines integrate seamlessly with upstream primary packaging and downstream serialization, enabling continuous production flow. We support both standard and complex configurations including multi-component kits and promotional packaging.

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Serialization & Track-and-Trace

End-to-end serialization, aggregation, and compliance reporting for DSCSA, EU FMD, and international regulatory frameworks including Brazil ANVISA, South Korea, and China. Our serialization infrastructure spans all packaging lines and supports real-time data exchange with trading partners and regulatory authorities through established EDI and portal-based connectivity.

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Cold Chain Packaging

Validated temperature-controlled packaging for biologics, vaccines, cell and gene therapies, and other temperature-sensitive pharmaceutical products. We maintain qualified cold rooms and controlled environments supporting storage and packaging at 2-8°C, -20°C, and -80°C. Every process is backed by documented thermal qualification protocols and continuous monitoring.

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Clinical Trial Packaging

Full-service clinical supply packaging for Phase I through Phase IV studies, including patient-specific kitting, randomization and blinding, comparator sourcing, and multi-country labeling. Our clinical operations team works directly with sponsors and CROs to deliver compliant, on-time clinical supply that supports enrollment timelines across global trial sites.

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Packaging Engineering & Design

Structural design, material selection, stability testing support, and full packaging validation aligned with USP, ASTM, and ISTA standards. Our engineering team partners with pharmaceutical manufacturers from early-stage development through commercial launch, optimizing packaging configurations for product protection, regulatory compliance, and total cost of ownership.

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INTEGRATED PLATFORM

An Integrated Approach to Pharmaceutical Packaging

Most pharmaceutical packaging challenges don't fit neatly into a single service category. A new product launch might require structural design and material selection from our engineering team, high-speed blister packaging on our primary lines, serialized cartoning through our secondary operations, and validated cold chain handling for temperature-sensitive distribution - all coordinated through a single project team and quality system.

That integrated capability is what sets Meridan apart. Instead of managing multiple vendors across different stages of the packaging process, our clients work with one partner who owns the entire workflow from incoming bulk product through finished, serialized, distribution-ready goods.

This single-source model reduces handoffs, eliminates inter-vendor coordination risk, compresses timelines, and provides a single point of accountability for quality and regulatory compliance.

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Common Multi-Service Programs

  • New Product Launch
    Engineering, primary packaging, serialization, and distribution packaging coordinated as a single program.
  • Biologics Packaging
    Cold chain handling, vial or syringe packaging, serialized secondary packaging, and validated shipping configurations.
  • Global Clinical Supply
    Clinical trial kitting, multi-country labeling, cold chain logistics, and randomization and blinding services.
  • Line Extension or Reformulation
    Packaging engineering for new configurations, stability testing support, and commercial packaging scale-up.

Ready to optimize your packaging operations?

Partner with Meridan for reliable, compliant pharmaceutical packaging at scale.

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