GenomeQuest Inc., a global provider of large-scale genomic software applications, announced today that it has awarded six grants totaling more than $120,000 in software and services to help six laboratories facilitate the transition from multiple Sanger-based gene tests to consolidated next generation sequencing (NGS) based tests.
The American Association for Clinical Chemistry (AACC) presents a webinar, Body Fluid Testing in the Clinical Laboratory, to be held on Wednesday, February 8, 2012 at 2:00pm Eastern and lasting 90 minutes.
Thermo Fisher Scientific Inc., the world leader in serving science, today introduced Unity™ Lab Services, a new offering that combines product and laboratory support services to create a single solution for customers to optimize productivity and reduce their total cost of laboratory operations.
QIAGEN N.V. announced today the launch of the QIAensemble Decapper automation system that will facilitate the handling of liquid-based cytology and various other types of liquid samples that are processed by clinical laboratories around the world.
NeTLIMS™ NJ, LLC, a provider of advanced Laboratory Information Systems (LIS), today announced that its clients are implementing and using new software that will allow them to comply with the HIPAA 5010 formats that have been mandated by CMS.
Based on input from many STARLIMS users, Forum2012 aims to address the interesets of labs in multiple industries and disciplines. Forum2012 is an opportunity to share know-how and to strengthen collaboration between the global STARLIMS community. The dates are March 6-9 in Fort Lauderdale, FL. Register today and enjoy discounted registration rates.
Genomic Data Analysis and Interpretation, Epigenetics, Comprehending Copy Number and Structural Variation, Targeting Non-Coding RNA, RNA-Seq, DNA-Seq, Sequencing Data Storage and Management, Successful Sequencing
Spanning five days this year, the event now includes more activities including: 2 partnering forums, 5 symposia, 18 short courses, and 12 core programs. Join over 3,000 attendees in interactive lectures, discussions, and various receptions as a way to facilitate networking opportunities and hearing differing views and perspectives on poignant issues facing you and our industry today.
This webinar covers production and QMS requirements for software (Excel spreadsheet) built into a medical device, as outlined in 21 CFR 820.70(i). Get practical advice on writing validation protocols and reports for Excel spreadsheets.
This 3-hr virtual seminar on OSHA Subpart Z (or IH) Regulations will discuss many of the individual standards as well as the general model and approach and “template” that OSHA takes with these IH regulations.
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