PHARMACEUTICAL

YOUR TRUSTED PARTNER FOR ANALYTICAL EXCELLENCE AND COMPLIANCE SOLUTIONS

PHARMACEUTICAL LAB

Triverity Laboratories delivers high-quality analytical development services and routine testing to the pharmaceutical industry. Our experienced scientists are committed to providing accurate, reliable and timely results to support your drug development and manufacturing needs.

We can support every stage of your drug development process. From early-phase method development to late-stage validation and stability studies, our team works closely with you to ensure robust and compliant analytical methods.

Our stringent quality control processes and adherence to regulatory guidelines ensure that our results are always reliable and reproducible. We follow Good Manufacturing Practice (GMP) regulations as outlined in 21 CFR Parts 210 and 211, maintaining the highest standards of quality in all our services. Additionally, we understand and comply with the regulatory requirements of the FDA, EU and TGA in Australia.

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CLIENT PARTNERSHIP

Our team of scientists brings decades of experience in pharmaceutical analysis, ensuring your projects are handled with precision and expert knowledge.

We believe in a collaborative approach to ensure the success of your products. By engaging in detailed discussions, we gain insight into your specific needs and goals. Based on this understanding, we design customized studies tailored to meet these requirements.

Throughout the process, we maintain open communication and provide comprehensive reports to support the results of our studies. These reports offer clear, actionable insights, ensuring that you have the data needed to achieve regulatory compliance and drive product development.

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