A multinational pharma group's Australian branch was manufacturing a medication that reduces infection risk following chemotherapy. The process involved UV Vis spectroscopy and a strictly documented workflow.
New regulatory demands showed the laboratory's QC manager that their current UV Vis spectroscopy equipment needed to meet workflow security, accuracy, and documentation requirements. The workflows had become so complex that they required a software solution and a qualified, validated UV Vis spectrophotometer.
The QC manager turned to METTLER TOLEDO's UV7 Excellence Spectrophotometer, which met all regulatory needs, including the updated United States Pharmacopeia (USP). Combined with LabX software.
The new system enabled the Australian lab to fully meet and exceed all their SOPs for sample preparation and accurate and repeatable absorbance measurements. The combined system supported the lab's staff daily, ensuring they could prepare and measure all samples using fully compliant methods. The staff received prompts directly on the instrument terminal, reducing errors.