WebInterstate Inc. Partners with Liaison Healthcare for EMR Integration with Mobile Radiology Providers
WebInterstate Inc., developers of MediMatrix™ and an industry leader in mobile imaging, is thrilled to announce new Electronic Medical Records (EMR) integration opportunities produced through a new strategic alliance with Liaison Healthcare, a global provider of secure cloud-based integration and data management services. Liaison's EMR-Link™ optimizes EMR workflows and integration for the ordering and reporting of diagnostic tests.
Biopreservation Market Estimated to Reach USD 5.69 Billion by 2019: Transparency Market Research
According to a latest market research report published by Transparency Market Research, a U.S-based market intelligence firm, a continuous rise in research activities in the field of biomedical sciences, rendered by the rising global demand for new medicines and medicinal therapies, will be one of the major factors leading to the growth of the global biopreservation market. The rising need for automation by storage facilities will allow growth in the sector of LIMS.
Best Practices With Submissions Under Medical Device User Fee Act (MDUFA) III
This webinar will present the results of the MDUFA III and will describe how your company will need to do business with the FDA in the next five years. It will describe how the FDA will use the User Fees to make changes within the agency and the expectations that the FDA will have of your company, as a result of those changes, to help your company prepare both strategically and tactically for regulatory interactions in the next five years.
Simulations Plus Releases ADMET Predictor Version 7.0
Simulations Plus, Inc., a leading provider of consulting services and software for pharmaceutical discovery and development, today announced that it has released version 7.0 of its best-in-class ADMET Predictor™ molecular property prediction software.
Essential Do’s and Don’ts for Navigating a Successful 505(b)(2) Drug Application
This FDA New Drug Approval process training will provide attendees with the knowledge and skills needed to develop a successful 505 (b)(2) program.
Understanding and Interpreting the EMA Reflection Paper on GCP Compliance in Relation to Trial Master Files (paper and/or electronic) for Management, Audit and Inspection of Clinical Trials
This training will give attendees an insight into the interpretation of GCP regulations by the European Medicines Agency (EMA) as they relate to the management of trial documents, focusing especially on clarification within the paper on disputed and ambiguous areas of trial master file (TMF) management.
Autoscribe – How to Buy a LIMS webinar
Autoscribe, a leading developer of Laboratory Information Management Systems (LIMS), has announced it will be running a series of three free �How to Buy a LIMS� webinars on 26th March, 23rd April and 28th May 2014. With over 60 years of practical management experience specifying and delivering successful LIMS solutions to any laboratory in any industry, Autoscribe has designed these webinars to provide information that will help keep anyone considering purchasing a LIMS on track, avoid some of the pitfalls and find the right solution to fit the specific needs.
Report Designs in LIMS do matter in today’s “visible” world
Most of us are not accomplished graphic designers - or photographers for that matter. But our clients still expect that we will produce easy-to-follow reports that can help them to communicate with other stakeholders how your laboratory is performing. One of the best ways to ensure that your reports have the information and look you want is to utilize the features inherent with report templates within a LIMS. You should have the choice to customize the look and feel that meet your needs and answer any questions your customers have.Blaze Systems Releases New Version of BlazeStability Shelf Life Study Product Available as a SasS Offering.
Blaze Systems announced a new release of its BlazeStability shelf life management software now available as a SaaS (Software as a Service) offering including end-to-end management of the entire study process, including storage and analytical functions. This development makes automation of the complete organization and execution of shelf life studies available to labs of all sizes, with a sea-change reduction in the entry barrier to getting on-line.
A New Concept In Screen Saving From Matrix Gemini LIMS!
The versatile ‘OneTime configuration tools’ provided with the Matrix Gemini Laboratory Information Management System (LIMS) from Autoscribe, not only allow the system to be configured without the use of custom programming, but also uniquely provide an audit trail each time a display screen for the system is updated or modified. If a screen is being altered, no one else can modify it until it goes live again. Each version is saved with a version number so the audit trail allows the possibility of returning to an earlier version if required.
Laboratory Informatics Weekly Update – Volume 12, Issue 11
March 26, 2014 Laboratory Informatics Weekly Update Volume 12, Issue 11 In This Issue Webcast Focus 04/23/2014 - Autoscribe - How to Buy a LIMS webinar Autoscribe, a leading developer of Laboratory Information Management Systems (LIMS), has announced it will be running a series of three free �How to Buy a LIMS� webinars on 26th March, 23rd April and 28th May 2014. With over 60 years of practical management experience specifying and delivering successful LIMS solutions to any laboratory in any industry, Autoscribe has designed these webinars to provide information that will help keep anyone considering purchasing a LIMS on…CAPA, Failure Investigation and Root Cause Analysis – FDA Expectations
This 90-minute webinar will show how you can implement a closed-loop CAPA system that meets CGMP requirements and U.S. FDA expectations. You will learn simple, but powerful, tools and methods that you can use regularly and systematically to define and resolve root causes, not just symptoms.
Understanding FDA Import Alerts: What Are They and Recommendations for Removing Your Company and Products from an Alert
This webinar will focus on the different types of import alerts issued by the FDA. It will provide the attendees strategic recommendations for removing one’s company and/or products from an import alert.
N-of-One and BioDiscovery Partner to Deliver Tumor Genomics Analysis and Interpretation Platform
BioDiscovery, Inc., a leader in DNA structural variant analysis laboratory software for copy number (CNV) and sequence variation, and N-of-One, the leading provider of molecular interpretation and therapeutic strategies for precision medicine in oncology, today announced a partnership to jointly provide integrated genomic analysis interpretation solutions.
Creating a Global Regulatory Plan
This regulatory training will help attendees understand key benefits for implementing and maintaining an effective global regulatory plan. Attendees will also gain exposure to the elements and a methodology for global regulatory plan development and maintenance.
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process
This webinar will discuss the different aspects which auditors generally look in equipment calibration, maintenance and validation and highlight the best practices.
The Regulation of Pet Food in the United States
This 90-minute training will provide an introduction to FDA’s rules governing pet food product development and formulation, manufacturing, labeling; and marketing and promotion. In addition to facility inspections and product recalls, the webinar will summarize and assess FDA’s enforcement activity in the U.S. pet food market paying particular attention to enforcement trends and risks.
NovoPath Anatomic Pathology Software Platform Receives 2014 ONC HIT Certification
NovoPath announced today that its NovoPath version 9.0 anatomic pathology laboratory information management software platform is compliant with the ONC 2014 Edition criteria and was certified as an EHR Module on February 14, 2014 by the Certification Commission for Health Information Technology (CCHIT®)
The Only Event Dedicated to Next Generation Lab Informatics Is Back!
The world of lab data and informatics systems is evolving. Make sure you stay up-to-date with the ELNs, Data Analytics and Knowledge Management (EDKM) Summit, taking place in Boston, MA from 17-18 June 2014. EDKM is the only meeting in the US that provides answers and real user case study experiences in laboratory informatics systems.
Social Media and Marketing FDA Regulated Products
The webinar will discuss the do’s and don’ts for using social media in marketing FDA-regulated products. Common issues, misconceptions, perceptions, and possible solutions will be discussed. The presentation will to familiarize you with the current FDA rules and help you plan for developments expected in the near future.
