Your Product

Your Product

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Your Product

Services tailored to your product, ensuring the right development path, scalable processes, and consistent manufacturing outcomes.

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Your Stage

Your Stage

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Your Stage

At each stage, new challenges emerge. A single team and site ensure continuity and consistent execution across the product lifecycle.

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Our Services

Our Services

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Our Services

Integrated CDMO services designed for seamless progression from development through commercial manufacturing, under global regulatory standards.

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Resources

Resources

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Resources

Technical insights, practical guidance, and applied expertise to support decision‑making at every stage.

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About Us

About Us

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About Us

An overview of Groupe PARIMA, our mission, and our expertise in supporting the pharmaceutical industry.

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    Labeling & Serialization

    We integrate labeling and serialization directly within manufacturing execution to support compliant commercial supply.

    Drug Manufacturing banner

    Labeling & Serialization for Global Supply

    We offer coordinated artwork integration, compliant labeling, and robust serialization to support accurate product identification, global traceability, and reliable batch release.

    Labeling and serialization are critical GMP operations that directly impact market access, traceability, and supply reliability. Groupe PARIMA provides integrated labeling, serialization, and artwork coordination services designed to align regulatory requirements with manufacturing execution, ensuring readiness for commercial distribution across multiple markets.

    Artwork Coordination

    We coordinate artwork through defined proofing and approval workflows to support compliant labeling.

    Labeling Solutions

    We manage GMP‑controlled labeling operations to support accurate product identification.

    Serialization and Aggregation

    Our capabilities support global regulations, enabling end‑to‑end product traceability.

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    Turn-key Execution

    We integrate labeling control, artwork coordination, and serialization capabilities within our packaging operations to support consistent, inspection‑ready execution.

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    Market Compliance

    Our team works hand in hand with yours to ensure approved artwork is accurately incorporated across products, formats, and markets.

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    Print‑File Readiness

    Print files are reviewed for GMP compliance and label readability to confirm accuracy and execution readiness prior to approval for use. 

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    Supplier Coordination

    Collaboration with qualified packaging suppliers ensures materials and components are selected and supplied within approved specifications.

    Labeling and Serialization Capabilities

    Groupe PARIMA’s labeling and serialization capabilities support accurate execution across regulated markets. Our technical approach combines packaging guidance, serialization control, traceability, and supplier coordination to ensure labeling operations remain aligned with client and regulatory expectations.

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    Packaging Design Guidance

    Technical guidance is provided on labeling and packaging layouts based on format constraints.

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    Unit‑Level Serialization

    Unique serial numbers are applied at the individual saleable unit level in alignment with defined serialization strategies.

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    Full Aggregation Support

    Serialization is supported with full aggregation across unit, bundle, case, and pallet packaging levels.

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    Traceability Data Management

    Traceability data is generated and managed for compatibility with client systems and third‑party track‑and‑trace providers.

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    Regulatory Data Exchange

    Serialized data is transmitted to support downstream regulatory traceability and product authentication.

    Our Numbers

    Our labeling and serialization metrics reflect the scale, regulatory reach, and operational consistency clients rely on when moving products to commercial supply.

    5 to 2,500 kg

    Batch Sizes

    Creams, gels, and ointments manufactured across development, scale‑up, and commercial production.

    20 to 4,000 kg

    Batch Sizes

    Liquids and suspensions produced at multiple scales to support clinical supply and commercial demand.

    30M Units

    Annual Capacity

    High‑capacity manufacturing operations supporting sustained commercial production.

    Labeling and serialization activities are executed in alignment with packaging specifications, serialized data requirements, and regulatory expectations from manufacturing to commercial distribution.

    Resources

    Our resources share practical insights on labeling and serialization to help clients make informed technical and regulatory decisions.

    Groupe PARIMA
    2026/04/27
    How Drug Product Formulation Works: Topical, Oral, and Nasal Liquid and Semi-Solid Dosage Forms
    Read more
    Groupe PARIMA
    2026/03/18
    How Early API Characterization Can Reduce Formulation and Scale-up Risks
    Read more
    Groupe PARIMA
    2025/10/23
    Topical 101: A Guide to Complex Dermatology Formulation Development
    Read more
    Groupe PARIMA
    2026/04/27
    How Drug Product Formulation Works: Topical, Oral, and Nasal Liquid and Semi-Solid Dosage Forms
    Read more
    Groupe PARIMA
    2026/03/18
    How Early API Characterization Can Reduce Formulation and Scale-up Risks
    Read more
    Groupe PARIMA
    2025/10/23
    Topical 101: A Guide to Complex Dermatology Formulation Development
    Read more

    See all Resources

    Contact Us

    Discuss your labeling and serialization strategy

    Let’s discuss how our integrated CDMO expertise supports compliant labeling and serialization execution from manufacturing through commercial distribution.