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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    Analytical Services

    Our in‑house analytical lab designs, optimizes, and validates methods for chemical and microbiological testing.

    Integrated analytical services

    Full lifecycle analytical support

    The analytical laboratory at Groupe PARIMA supports every stage of the product lifecycle, from pre-formulation studies to commercial release. Our team applies technical and scientific expertise using qualified equipment to ensure that every method, test, and data set contributes to the product’s safety, efficacy, and regulatory compliance.

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    Quality driven by analytical data

    Our integrated analytical support ensures product quality and acts as a strategic enabler across the development and manufacturing of pharmaceutical products. 

    Faster decision‑making

    Direct access to analytical teams reduces turnaround times, accelerates issue resolution, and keeps development and manufacturing moving forward.

    Data continuity and control

    Analytical methods, results, and trends are managed within the same quality system, ensuring consistency, traceability, and full ownership of your data.

    Stronger regulatory readiness

    Analytical expertise aligning development, validation, and manufacturing, strengthening documentation, and streamlining regulatory interactions.

    By generating reliable, regulatory-ready data, our laboratory helps ensure that products maintain their safety, efficacy, and quality throughout their shelf life.

    Analytical Precision

    Whether developing new analytical methods, transferring an existing one,  executing routine testing, or monitoring stability programs, our laboratory operates with precision and reliability. 

    Method Development
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    Method Validation
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    Release Testing
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    Stability Studies
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    method development

    Designing fit‑for‑purpose analytical approaches

    Custom analytical methods tailored to the unique physical and chemical properties of each product, enabling precise characterization and reliable performance.

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    method validation

    Establishing reliability and regulatory confidence

    Comprehensive validation in accordance with ICH guidelines, assessing accuracy, precision, specificity, linearity, range, and robustness.

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    Release Testing

    Batch release driven by validated testing

    All testing is conducted under full GMP compliance and tailored to the specific requirements of each product and process.

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    Stability Studies

    Stability data for confident shelf‑life decisions

    Stability studies define shelf life and storage conditions, with full traceability and documentation to meet regulatory expectations. 

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    Core Analytical Capabilities

    Our in-house equipment supports stage-appropriate method development and routine testing across chromatography, particle sizing, physical testing, and dissolution.

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    Complete Laboratory

    Comprehensive in-house instrumentation to support method development, data integrity, and reliable routine testing.

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    Chromatography tools

    Chromatography runs under Waters Empower 3, supported by HPLC, UPLC, GC headspace, and LCMS for robust chemical characterization.

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    PSD analysis

    Particle and droplet size testing using Malvern Mastersizer and Spraytec, supported by microscopy for formulation and performance characterization. 

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    Physical testing

    Physical characterization, including viscosity and basic rheology using Brookfield viscometers, plus complementary measurements such as pH and water content.

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    Dissolution testing

    Dissolution testing to evaluate drug release performance and support method-driven control strategies across development and routine testing.

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    IVRT testing

    IVRT testing using Franz diffusion cells to characterize drug release kinetics for semi-solid drug products.

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    Autotitration testing

    Automated titration provides validated endpoints for assay methods, such as acid-base titration or redox titration.

    FAQ

    Below are answers to the most common questions we receive regarding our analytical services.

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    What is an analytical service?

    An analytical service refers to laboratory activities used to assess the identity, quality, strength, purity, and stability of pharmaceutical products. At Groupe PARIMA, analytical services support product development, manufacturing control, and regulatory compliance by generating robust data for formulation development, process monitoring, release testing, stability studies, and global regulatory submissions.

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    What analytical services should a pharmaceutical CDMO provide in‑house?

    A pharmaceutical CDMO should provide core analytical services in‑house to support development, manufacturing, and regulatory requirements effectively. At Groupe PARIMA, this includes analytical method development and validation, routine and stability testing, release testing, and analytical support throughout scale‑up, technology transfer, and commercial manufacturing, ensuring alignment with production processes and quality systems.

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    Why is in‑house analytical testing important for regulatory compliance and tech transfer?

    In‑house analytical testing is critical for maintaining data integrity, ensuring method consistency, and enabling reliable technology transfer across development and manufacturing stages. At Groupe PARIMA, integrated analytical testing strengthens regulatory compliance by preserving method knowledge within a single quality system, supporting consistent documentation, and meeting the expectations of global health authorities during submissions, audits, and inspections.

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    Start with integrated analytical expertise

    Partner with a CDMO that embeds analytical services directly into development and manufacturing to ensure continuity, quality, and long‑term program success.

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