Validation CSV, Laboratory, Devices, Process, Product, Cleaning, IT, labs Our laboratory instrumentation exposure not only includes a strong analytical testing repertoire but experience in system validation activities for research laboratories, such as drug discovery, analytical development, pharmacy development, formulations, new drug development, technical transfer, physical pharmacy, microbiology, genomics, toxicology, immunology, hematology, auto-chemistry, robotics, raw materials exploratory studies, clinical trails, product release, and more.
Facilities, Utilities and Equipment Our commissioning and qualification team has the experience and technical skills to ensure our clients’ facilities meet or exceed regulatory requirements. We are able to quickly identify needs and solutions and will work with the clients’ team to complete the project within budget, boundaries and expectations. VQS will develop commissioning documents to verify proper installation and optimum performance We will •provide project management tools, processes, and principles to enable successful project execution. This includes managing project goals to ensure we are within scope, on budget, and on schedule. •Work on multi-discipline engineering capital project teams, as well as other project-related, cross-functional teams. •Measure and report project execution progress. Decision-making and make influential recommendations regarding best options. •We have had the opportunity to design, develop, install, assess, remediate, validate, qualify, retire and automate hundreds of different types of instrumentation. We have years of extensive experience on computer networks and laboratory instrument integration IQ, OQ, PQ, DQ, SOP, and more. We have a strong background in validating Laboratory Systems, Building Utilities, BMS, SCADA, DCS and PLC systems. With us you do nothing! VQS will write and managed execution of cleaning validation, protocols, analyzed microbiological, visual, analytical and physical data to detect trends and develop corrective actions as necessary. VQS will write validation report summarize results and findings. Review and analyzed cleaning records, detected negative trends and non-conformances, and developed and implemented process improvements as needed.