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We provide industry-leading production know-how and comprehensive regulatory support for high-quality active pharmaceutical ingredients (APIs), backed by nearly 200 years of experience. Our commercial and late-stage APIs, as well as advanced intermediates, are primarily manufactured and purified at our cGMP site in Arklow, Ireland. The 64,000-square-meter facility includes extensive processing equipment, milling capability, testing laboratories, and state-of-the-art fractional distillation equipment. We have the resources and technical expertise to support you with new process evaluation, product registration and filing, process development and validation, technology transfer, reference standard synthesis, and regulatory filing support.