April 22, 2014 - 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.

April 22, 2014 - 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.

April 22, 2014 - 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).

April 18, 2014 - 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.

April 17, 2014 - 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.

April 17, 2014 - 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.

April 17, 2014 - 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.

April 17, 2014 - 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.”

April 16, 2014 - 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.

April 16, 2014 - 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.

April 16, 2014 - 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.

April 16, 2014 - 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.

April 16, 2014 - 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.

April 15, 2014 - 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

April 15, 2014 - 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

April 15, 2014 - 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.

April 15, 2014 - 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

April 11, 2014 - Elements of an Effective Change Control System

This webinar will focus on the regulatory and design requirements for an effective change control system. Attendees will learn role and importance of change control system in implementing an effective quality system.

April 10, 2014 - The NCPDP Standards and Understanding Unique Healthcare Transactions

This webinar on healthcare transactions and its compliance requirements will help you navigate the NCPDP standards and discuss the pitfalls you need to avoid while implementing it.

April 9, 2014 - Illumina Expands Product Portfolio to Support Oncology Clinical Research and Discovery

Illumina, Inc. announced new products that can be applied directly to the discovery and translation of genomic variation in blood and tissue associated with cancer. The expanded portfolio leverages the company’s industry-leading next-generation sequencing (NGS) and microarray scanning systems to deliver sample-to-data solutions for basic and clinical cancer research.