With state-of-the-art facilities, equipment and techniques, Pharmalytics incorporates industry best practice at all times. With full audit trails, electronic signatures, and an integrated electronic quality management system, you can be assured your analytical results and data are safe and secure.
US FDA FEI: 3016044111
Pharmalytics employ a full 21 CFR Part 11 electronic quality and documentation system. Every single thing we do is electronic. And we’re the only pharmaceutical contract testing laboratory in the country that operates to this standard. Put simply, we have removed manual recording, redundant processes and human error from the equation. All electronic records are database driven, locked, secured and cannot be altered – and each analysis, performed by a method, can only be recorded by trained and qualified analyst for your samples.
Pharmalytics is a first-to-market partner for Agilent Technologies and Mettler Toledo.
Agilent Technologies is a global leader in the supply of instruments, services and consumables for the life sciences, diagnostics and applied chemical markets. Their end-to-end portfolio enables reliable, precise answers for all stages of a product’s lifecycle and ensures excellence, optimal performance and robustness for Pharmalytics at all times.
Mettler Toledo precision instruments are renowned in laboratories all over the world for the accuracy of their results. Thanks to their partnership, Pharmalytics can reliably deliver innovations in performance, measurement techniques and evaluation procedures to analyze contents, concentrations, material properties and compositions. Our Mettler Toledo instruments, combined with LabX software, fully support the current requirements of regulatory bodies including the TGA and FDA under a 21CFR Part 11 compliant framework.
Just 40 minutes from Melbourne’s airport and CBD, the Pharmalytics lab offers the latest