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We consider ourselves leaders in the analysis of raw materials, both excipients and active pharmaceutical ingredients (APIs) as well as some finished products, to international pharmacopoeial specifications in accordance with cGMP.

With the majority of our work focused on ensuring the quality in the production and manufacture of medicinal products, our analysts are trained to perform every task with the safety, well-being and protection of the patient foremost in consideration. Consequently, we are confident that all of our services are provided to the highest quality standards.

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The latest technology combined with our expert team of scientists make us leaders in Quality Control Testing, Method Development, Method Validation and Stability Testing of both pharmaceutical raw materials and finished products.

We refine this service by promoting a culture of open communication between our analysts and our clients, ensuring that you retain control of your work.

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