Conducting a Risk Analysis to Comply with Meaningful Use, HIPAA and HITECH
This webinar will discuss how to do a security risk analysis to meet the requirements of HIPAA, HITECH and Meaningful Use attestation. It will describe ways for effectively completing a risk analysis at the organizational level, the network level and the application level.
Medical identity theft: What you don’t know could destroy you
This webinar will help you understand the basics of identity theft, highlight ways in which identity theft happens, how to reduce exposure, as well as integrate into a well designed compliance program that strengthens the company's ability to grow and meet critical privacy laws.
Major Changes to the EU Clinical Trials Regulation: What is Required for Compliance
This webinar will help Sponsors, CROs and study sites running clinical trials in the EU and internationally; understand the important, updated compliance requirements concerning the new EU Clinical Trials Regulation due to be enacted in 2016 and which will replace the 2001 Clinical Trials Directive (CTD) (2001/20/EC).
Professional advice to manage the efficiency of your lab
If you will sit and start making a list of things which are keeping your lab from being productive the list will go quite a long. There are so many electronic deliverable which can manage the data of your lab to make it more productive.Sources Sought – Laboratory Automation System
Agency: Department of the Navy, Office: Bureau of Medicine and Surgery. Navy Drug Screening Laboratory - Great Lakes is interested in automating some or its entire sample accessioning process.Regulatory Documentation for Clinical Trials
This clinical research compliance training will explain in detail the list of required regulatory documentation for clinical trials for industries such as pharmaceutical, biotechnology, medical devices and diagnostics. It will also review many of the documents in terms of required content and structure.
Selerant Launches Regulatory Compliance Cloud Service for the Food Industry Online Regulatory Issue Database
Selerant (selerant.com) announced today that it has launched a new online subscription service at compliancecloud.selerant.com. This new service provides immediate access to thousands of food legislation records, news and alerts that are vital to ensure safety and compliance of food products.
Design Considerations for Pivotal Clinical Investigations for Medical Devices
This webinar will explain in detail the FDA guidance on design considerations for pivotal clinical investigations for medical devices. It will discuss the regulatory considerations for clinical study design, including the ways for eliminating bias and variance that may impact the quality of the data obtained in the study.
Benchmarking Your Company’s Safety Performance, Or That of a Potential Contractor against Companies in the Same Industry
This OSHA compliance webinar will explain how to compute safety performance measures for your own company or your existing and potential contractors. Attendees will learn best practices to avoid OSHA fines and penalties.
Legal Issues Surrounding Hospital and Physician Relationships
This webinar will explain the relationship both historically and currently between a hospital, its medical staff and its physicians. It will help attendees understand what is required by the hospital and its medical staff to meet the requirements of the “corporate responsibility doctrine.”
Forensic Labs – A Strong Case for LIMS
CSols, Inc. Complementary Webinar: dive into the forensic informatics world, reflecting on the benefits of a forensic LIMS and learning concepts and methods for your LIMS to reach its highest potential.
Research and Markets: Global Laboratory Information Systems (LIS / LIMS) Market 2017 – Clinical Laboratory Software and Hardware, Drug Discovery Systems
Research and Markets (http://www.researchandmarkets.com/research/trkb23/laboratory) has announced the addition of the "Laboratory Information Systems (LIS / LIMS) Markets - Clinical Laboratory Software and Hardware, Drug Discovery Systems" report to their offering.
The Microbial Factor of Non-Sterile Cleaning Validation
This webinar will focus on the microbiological element of non-sterile manufacturing cleaning validation and the need to design a robust cleaning routine. It will address the different pharmacopoeia regulations and current regulatory trends. It will also cover the theory in setting the baseline profile and limits along with determination of routine testing.
Design Inputs – Design Outputs Traceability Matrix – Principles of Lean Documents and Lean Configuration
This webinar will explain how to apply the theory of lean documents and its corollary theory of lean configuration to present a fresh approach to these linked and cascading documents.
LIMS Configured And Implemented Within 3 Months
A new case study has been published by Autoscribe (http://tinyurl.com/pkl8d4h), which highlights how its Matrix Gemini Laboratory Information Management System (LIMS) was configured and implemented in just 3 months at global paper supplier, Glatfelter. Glatfelter’s corporate analytical services group offers a wide range of analytical capabilities with some 15 instruments available. The laboratory performs multiple functions ranging from product development and process improvements to environmental analyses.
Laboratory Informatics Weekly Update – Volume 12, Issue 14
April 16, 2014 Laboratory Informatics Weekly Update Volume 12, Issue 14 In This Issue Articles Productivity Is A Must When Managing The Efficiency Of Your Lab Think of all the features and characteristics that may be keeping your lab from being as productive as possible. The list could be extremely long. In today’s lab environment these aren’t roadblocks but are merely challenges. At the highest level, what you are likely faced with is too much manual work for your staff and some operational processes that are inefficient or time consuming. Webcast Focus 04/23/2014 - Autoscribe - How to Buy a…Risk based Computer System Validation for SaaS/Cloud/Local Hosting
Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable
GE Healthcare Completes Acquisition of Analytics Solutions Provider CHCA
GE Healthcare announced today it has completed the acquisition of CHCA Computer Systems Inc., an operating room (OR) management and analytics solutions provider, headquartered in Montreal, Canada. CHCA develops the leading Opera software application
Centice Announces the Release of Version 5.5 of its Drug Identification Software with Significant New Additions to the Illicit Database
Centice Corporation, a pioneer in narcotic and pharmaceutical identification using Raman spectroscopy technology, today announced the release of version 5.5 of its drug identification software.
Laboratory Information Systems (LIS / LIMS) Markets (Clinical Laboratory Software and Hardware, Drug Discovery Systems)
Laboratory information systems (LIS), also known as laboratory information management systems (LIMS), are data and information management systems designed for industrial and medical-related laboratories, including clinical and analytical laboratories. This Kalorama Information market report, The World Market for Lab Information Systems (LIS) analyzes the current and potential world markets for medical laboratory information system software and hardware
