ARIREX is a consulting, compliance, and auditing firm dedicated to elevating operational standards across pharmaceuticals, biologics, food and beverage, medical devices, natural health products, cosmetics, and other regulated industries. Built on a foundation of integrity, technical excellence, and evidence-based decision-making, we provide clarity in highly controlled environments.
Partnering with global pharmaceutical and biotech leaders to ensure regulatory success.
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Our approach is methodical, transparent, and grounded in real-world experience.
Our commitment is reflected in our core strengths.
Across manufacturing, quality, regulatory affairs, and distribution.
Supporting both routine operations and high-stakes regulatory interactions.
Ensuring recommendations are not only compliant but also efficient and scalable.
Ensuring clients remain compliant as regulations evolve.
Ensuring systems meet or exceed expectations from FDA, EMA, Health Canada, and other global agencies.
Supported by industry best practices and internationally recognized guidelines (ICH, ISO, USP).
Ensuring recommendations are not only compliant but also efficient, scalable, and sustainable.
Working closely with clients to understand their unique processes and navigate regulatory challenges.
At ARIREX, we believe that compliance is a strategic advantage that strengthens an organization’s credibility, market access, and long-term resilience. We work collaboratively to build and reinforce systems that enhance traceability, reduce risk, and support a culture of quality.
With a strong presence in Canada and the capability to support clients across North America, Europe, and international markets, ARIREX is committed to being a trusted partner throughout your compliance journey.
Whether you are preparing for an inspection, expanding into new markets, or strengthening your internal quality systems, ARIREX provides the insight, structure, and leadership needed to move forward with confidence.