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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    About us

    A fully integrated CDMO with deep pharmaceutical expertise from development to commercialization.

    Pharma expertise across every stage

    Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO) specializing in non-sterile liquid, suspension, and semi-solid drug products.

    With over 30 years of experience, we support pharmaceutical and biotech companies with the development, manufacturing, and packaging of non-sterile drug products.

    We bring key services together under one roof, helping clients reduce handoffs, maintain alignment across stages, and move programs forward with confidence.

    Get to know Groupe PARIMA

    From our history and values to the people and culture that shape our operations, see what sets Groupe PARIMA apart.

    Our story
    Our Team
    Why groupe parima
    ESG+
    Career
    Our Story

    Experience shaped over time

    Over the years, we have developed an expertise in the development and manufacturing of pharmaceutical products.

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    Our team

    People behind the work

    Every position at Groupe PARIMA has a real impact and contributes to the success of our operations.

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    Why groupe parima

    What sets us apart

    We work closely with clients to deliver reliable execution and on-time delivery, acting as a true extension of their team.

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    ESG+

    Sustainable development

    Sustainability is embedded in our operations, with a focus on continuous improvement.

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    Careers

    Your next step

    Explore our open positions and take the next step toward a career defined by purpose, innovation, and growth.

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    Our Services

    As a fully fee‑for‑service CDMO, our operations are aligned with our clients’ objectives throughout the drug product lifecycle.

    01
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    Product Development

    Formulation and process development tailored to non-sterile small molecule drug products.

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    Analytical Services

    Method development, testing, and analytical support across development and manufacturing.

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    03
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    Manufacturing & Packaging

    GMP manufacturing and packaging for clinical and commercial supply.

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    Our numbers

    Our manufacturing capacity and global reach reflect deep experience, operational strength, and long-term commitment.

    30M+

    Packaging capacity

    Our facility is designed to scale production and support early packaging capacity.

    45+

    Countries served globally

    Our clients rely on us to bring their products to global markets on time and with quality.

    30+

    Years of experience

    Robust operations built for reliable delivery and efficient day-to-day execution.

    FAQ

    Learn more about us through quick answers to common questions about what we do and the products we support.

    01.

    Which regulated markets does Groupe PARIMA support?

    Groupe PARIMA operates under a GMP-compliant facility in Canada and holds a current Health Canada Drug Establishment Licence. We support products supplied to regulated markets globally, including Canada, the United States, Europe, Australia, New Zealand, and Turkey.

    02.

    What CDMO services does Groupe PARIMA offer?

    Groupe PARIMA supports the full drug product lifecycle, from development to commercial manufacturing and packaging, with integrated analytical, scale‑up, transfer, and testing capabilities.

    03.

    What types of drug products does Groupe PARIMA specialize in?

    Groupe PARIMA specializes in non-sterile small molecule drug products across liquid and semi-solid dosage forms, supporting oral, topical, nasal, and otic applications.

    04.

    Which development and manufacturing phases does Groupe PARIMA support?

    Groupe PARIMA supports programs from early-stage development through clinical supply, scale-up, technology transfer, and commercial manufacturing. Our integrated teams and on-site capabilities are designed to support the product lifecycle from pre-formulation studies and analytical development to commercial release.

    05.

    What career opportunities are available at Groupe PARIMA?

    Groupe PARIMA offers career opportunities across pharmaceutical development, quality assurance, operations, and administrative functions. Our company fosters a collaborative environment where continuous learning, knowledge sharing, and professional development are built into the way teams work.

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