QA/QC is an integral aspect of our analyses and is a key component to Actlabs’ vision, strategy and mission. Actlabs’ Quality System monitors all steps and phases of our operations. Our Quality System outlines comprehensive details concerning our facilities, personnel qualifications and processes used. Additionally, we are routinely audited by four regulatory agencies that focus on continual improvement. As a result, we continue to raise the bar with respect to quality of our services in order to exceed both their expectations and that of our customers. Our Quality Assurance program covers all areas of sample transportation, collection, preparation, analysis and data reporting.
Actlabs has a defined policy that ensures that all staff working in our laboratories are competent to perform the work required. New employees are trained to perform specific tasks and their ability to perform these tasks is formally assessed. Staff is routinely evaluated and up-to-date training and performance records are maintained.
Actlabs’ accredited in-house methods are fully validated before being used on client samples. Our customers are regularly challenging us to help them solve their analytical and quality problems. In addition to routine analyses, we develop and validate novel approaches that provide accurate and consistent results, and are of the highest quality.
Actlabs routinely monitors and documents the reliability of our sampling from the sample preparation process. This ensures that sub-samples taken are reliable and representative of the original sample submitted.
Many of the methods used at Actlabs are internally developed and validated to ICH or ISO 17025 guidelines. Actlabs also performs testing according to internationally recognized standards provided by standardization associations including ASTM, EPA, AOAC, ISO, FDA, USP or SAE.