Today at SLAS 2014, IDBS announces enhanced screening and analysis functionality in ActivityBase XE 7.7. The latest release addresses growing assay volumes for high content and multiparametric datasets by processing information up to 50 times faster than the previous version. In addition, new visualizations and third-party integrations support image-based screening capabilities and faster analysis to support decision-making.

Lab Managers attending the Society for Laboratory Automation and Screening (SLAS) conference and exposition are getting their first look at Thermo Scientific Momentum 3.3 automation scheduling software, which offers new features to facilitate set-up and streamline workflows.

LifeMap Sciences, Inc., a subsidiary of BioTime, Inc. (NYSE MKT: BTX), announced today the release ofLifeMap Discovery™ version 1.5 (discovery.lifemapsc.com). LifeMap Discovery™ is a state-of-the-art roadmap of embryonic development and stem cell biology.

Understand the steps of a extractables / leachables study, get knowledge about the gap analysis of literature sources and how to design an efficient E/L study.

This OOS Investigation training will review the various items that should be included in the investigation to determine the cause of the limit excursion for both viable and non-viable excursions.

This 90-minute cleanroom contamination control training will review the common mistakes that people make in cleanrooms that lead to contamination, show how to develop a successful contamination control program and discuss ways to improve your facility's design and maintenance.

This OSHA Recordkeeping training will address the key concepts in understanding the OSHA recordkeeping analysis through recent OSHA Interpretation Letters. This training will include hypothetical fact scenarios that present common recordkeeping issues encountered by facility record keepers.

This training will discuss regulatory requirements for monitoring of pharmaceutical impurities. It will explain how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and to measure the thresholds to report for regulatory submission.

This training on healthcare compliance will teach the attendees best practices for conducting a self audit of financial relationships with physicians. It will help you understand the key legal implications of Stark and Federal Anti-Kickback statutes.

This webinar will show how you can devise a clinical trial billing system/ process to manage the billing of clinical trial charges in compliance with Federal rules and regulations.

This training on FDA software validation related warning letters will discuss what to do to avoid additional software related compliance issues along with the response steps where the citations that directly or indirectly include automated system.

Companies face many common issues or confusions that arise while creating a validation program such as : Though company has expertise in process validation but never quite able to keep up with facility and equipment changes requiring never ending equipment qualification (IQ, OQ, PQ)

Integrating the requirements of 21 CFR 820 into a product development process is challenging. Done poorly, it drags down the design process and puts you a

Get trained on how to define the residual risk of medical device and how to streamline the software verification process by employing a risk based approach. You will learn Learn the best practices to ensure compliance with ISO14971 and IEC62304 regulations.

A growing public demand for supplements has resulted in a flurry of companies creating and marketing dietary supplements in the United States, EU and Canada. With the regulatory authorities beginning to take a stronger stance on enforcement of regulatory policies, procedures and GMP compliance, it is important for companies to verify that their products comply with the latest regulations and provisions if they plan to market Supplements in these countries.

InterSystems, a global leader in software for connected care, today announced that NHS Wales has successfully completed the first phase of the national roll out of InterSystems TrakCare® Lab, a comprehensive, multidisciplinary laboratory information management system (LIMS). The first phase of the implementation, covering all four labs in the Hywel Dda Health Board, is a major step in one of the largest and most complex pathology modernisation programmes in the western health economy.

Year-over-year PepTalk: The Protein Science Weekcontinues to draw leaders of biotherapeutics from industry and academia pioneering the evolution of biologics. The international delegation is comprised of over 1,200 participants from 20+ countries.

This 90-minute webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.

CLC bio, a QIAGEN company (NASDAQ:QGEN)(FWB:QIA), today announced in collaboration with Korilog the release of the KLAST plug-in for CLC Genomics Workbench and CLC Main Workbench to accelerate the analysis of data from next-generation sequencing (NGS).

Eyelit Inc., a manufacturing software provider for visibility, control, and coordination of manufacturing operations for the aerospace & defense, discrete electronics, life sciences, MEMS, semiconductor, and photovoltaic (solar) industries, announced today the general availability of version 5.1 of its Eyelit Manufacturing™ suite of software.