Accelrys, Inc. (NASDAQ: ACCL), a leading provider of scientific innovation lifecycle management software, announced today thatCambridge Isotope Laboratories, Inc. (CIL) is deploying the Accelrys Laboratory Execution System (LES) and three applications within the Accelrys Laboratory Information Management System (LIMS) to enhance quality control and regulatory compliance as the company experiences increased demand for its products

Agilent Technologies Inc. today announced it will host a series of scientific presentations at the annual meeting of the International Association of Forensic Toxicologists (TIAFT), Sept. 2-6, in Madeira, Portugal.

AB SCIEX, a global leader in analytical technologies, today announced the launch of MasterView™ Software, a new software application with built-in automation that quickly turns enormous amounts of complex analytical data into simplified, meaningful answers for safer food, cleaner environments and more reliable forensic drug screening than alternative approaches.

Life Technologies Corporation (NASDAQ: LIFE) today announced the first end-to-end sequencing solution for exon-level copy number variation (CNV) analysis, which combines the Ion Reporter™ CNV data analysis workflow, the Ion AmpliSeq™ Exome Kit and theIon Proton® System.

Faced with declining reimbursement and shrinking lab budgets, most clinical laboratory organizations are struggling to stay financially solvent. That is why a record-breaking lab industry event is expected when the nation's best cost-cutters in clinical laboratory and anatomic pathology testing gather in New Orleans on October 1-2, 2013 for the seventh annual Lab Quality Confab and Process Improvement Institute

This two day interactive in-person seminar will provide participants the regulatory background and guidelines through all critical areas of GMP compliance. This course helps attendees understand the latest requirements and also provides them templates and examples to develop inspection ready documentation.

This lab compliance training will provide an easy to follow outline for developing and updating the required HHS Laboratory Compliance Plan for any provider who bills Medicare or Medicaid for services.

STARLIMS today announced the launch of Version 11 Laboratory Information Management Systems (LIMS) software, available now worldwide. Based on Abbott’s Informatics Solutions, Version 11 will expand user functionality to include mobile device applications, advanced analytics and HTML5 compatibility. These features will allow STARLIMS users to work on the right screen for the task with an expanded platform to access LIMS information anywhere.

This webinar will provide a comprehensive overview of the new HIPAA Breach Notification rules, tips for preventing and preparing for breaches, the new penalties for non compliance, and how to prepare for HIPAA audits. It will include case-study discussions to explain the key elements in an HIPAA audit.

CSols Webinar: Learn the criteria to consider when deciding which Lab Informatics solution is the best fit for you.

Simulations Plus, Inc., a leading provider of simulation and modeling software for pharmaceutical discovery and development, today announced that it has released Version 8.5 of its industry-leading GastroPlus™ software program for the simulation of gastrointestinal absorption, pharmacokinetics, and pharmacodynamics.

Tests built within a Laboratory Information Management System (LIMS) generally define specific components within a test. However, there are occasions when users need to capture results for some unexpected or unplanned components of interest that may appear during the testing process. This is particularly true for chromatographic tests when unexpected peaks may materialize. To accommodate this need, Autoscribe has introduced an ‘Adhoc data entry’ facility into its Matrix Gemini LIMS.

Medical device manufacturers can avoid FDA Warning Letters, 483s and enforcement actions with a good understanding process validation principles. But knowing how to proceed is the toughest task as no FDA guidance document is available which talks about it.

This FDA software validation training will discuss how to approach strategic software validation planning so as to satisfy FDA by complying to new enforcement initiatives by FDA.

With a full schedule of conferences though the close of 2013, NovoPath, an industry leader in anatomic pathology (AP) lab management and reporting IT solutions, continues its ongoing support of laboratory medical professionals and the lab software industry. From its flagship NovoPath AP laboratory information system (LIS) to its sophisticated business tools, the company brings a range of its leading edge technology to these events and is an active participant in both formal and informal educational opportunities and in an exchange of ideas on the benefits of lab burgeoning technologies. Every year NovoPath takes part in a wide range of leading conferences covering a broad cross section of the industry on both a national and local level.

QPS a leading preclinical and clinical CRO, has now fully validated LabLogic Debra version 6.0.6 for use in radiolabeled metabolism studies. An earlier version was implemented in 2010 to support discovery stage radiolabel ADME studies.

CompuGroup Medical US, developer of CGM LABDAQ® Laboratory Information System (LIS), the nation's leading laboratory information system, is proud to announce the launch of CGM Endeavor. CGM Endeavor is an LIS designed to meet the specific needs of reference laboratories.