For researchers and technicians in clinical laboratories, especially those that serve the emerging fields of translational and personalized medicine, Thermo Scientific Clinical LIMS (laboratory information management system) software is designed to combine the sample-centric functionality of a LIMS with the patient-centric functionality inherent in a traditional LIS.
RURO and Appistry are please to announce partnership to deliver integrated solutions for Big-Data Lab Management for Production-Scale NGS. Automation is a fact of life for modern labs. But effectively managing the increasingly ubiquitous handoffs between humans, instruments, and computers requires ways to expedite and support both the physical work performed in the lab and the associated digital tasks performed by a lab’s computational workers. This is particularly important for labs seeking to provide results and diagnostic insights from data-intensive techniques such as NGS.
AB SCIEX, a global leader in analytical technologies, today announced the availability of MPX™ TF 1.0 Software to accelerate drug screening with accurate mass-based technology for laboratories performing clinical research. The new software is designed to deliver faster turnaround times, increased sample throughput and lower costs compared to single-stream, mass spectrometry (MS) methods.
Roche announced plans today at the AACC 2013 Clinical Lab Expo for the U.S. introduction of the cobas 8100 automated workflow series, an advanced system designed to automate many routine tasks to help diagnostic laboratories increase efficiency, reduce expenses and maximize patient safety.
TriCore Solutions, the application management experts, today announced that Nationwide Laboratory Services has chosen TriCore Solutions to transform their IT infrastructure by implementing a virtualized cloud-based information technology platform for all their managed services, infrastructure services and strategic consulting services.
Join 150+ drug R&D teams for practical discussions, solutions and case studies for refining early-stage drug discovery methods at four co-located conferences: Engineering Functional 3-D Tissue Models, Phenotypic Drug Discovery, Screening and Functional Analysis of 3-D Models, and Physiologically-Relevant Cellular Tumor Models for Drug Discovery.
With the tremendous expense of bringing new drugs to market, a focus on improving the outcome of first-stage research is critical. Recent evidence confirms the need for innovative screening systems utilizing assay design on three-dimensional tissue models and phenotypic models. This functional analysis will allow for more accurate biological response. Cambridge Healthtech Institute is pleased to introduce FAST: Functional Analysis & Screening Technologies Congress to bring together drug research and development teams for practical discussion, solutions and case studies for refining these first-stage drug discovery methods.
ILMAC is an internationally recognized tradeshow for process and laboratory technology from the fields of pharmaceuticals, chemistry, food, beverages, cosmetics and biotechnology. ILMAC 2013 covers all the industrial applications of process engineering, including research, development, production, and environmental engineering. This trade show is an excellent opportunity to establish and nourish networking connections in Europe.
This lab compliance training will provide an overview of the principles and requirements of ISO/IEC 17025, followed by some strategies and tool kits to assist laboratories prepare for and maintain accreditation by an ILAC-recognized accreditation body. This session will identify free resources available to laboratories to better understand the requirements of ISO/IEC 17025 and more easily implement them into their own laboratory QMS.
This training on bio-analytical methods validation will help you understand the clear, consistent and compliant approaches for instrumental, ligand binding, and cell based methods. A comparison of EMEA and FDA guidances will be presented.
This webinar will explain the cGMP and ICH validation requirements for analytical procedures and discuss key factors that would affect validation process of analytical procedures. It will review the differences between validation and re-validation plan.
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