Improving the creation and reporting of structured findings during digital pathology review
In this 2016 paper published in Journal of Pathology Informatics, Cervin et al. look at the state of pathology reporting, in particular that of structured or synoptic reporting. The group write about their prototype system that "sees reporting as an activity interleaved with image review rather than a separate final step," one that has "an interface to collect, sort, and display findings for the most common reporting needs, such as tumor size, grading, and scoring." They conclude that their synoptic reporting approach to pathology + imaging can provide a level of simplification to improve pathologists' time to report as well ability to communicate with the referring physician.
Justifying a New LIMS When You Already Have One
It is hard to justify the purchase of a new LIMS when you already have one in place. This blog discusses how to develop your LIMS justification by looking at the Functionality and Technology based Quantitative measures as well as Qualitative, and how to Calculate ROI.Justifying a New LIMS When You Already Have One
Appistry Extends Solutions for Next-Generation Sequencing Data Analysis
SEPTEMBER 20 – 23, 1026: ILMAC 2016
AUGUST 21 – 25, 2106: ISCB Conference 2016
AUGUST 17, 2016: CLSI Webinar: Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems
AUGUST 17, 2016: Sentinel Level Laboratory Updates: Keeping You in the Loop
IDBS provides bespoke software to Cancer Research Technology to streamline plate correction
Illumina and FlowJo, LLC Partner to Develop and Co-Market a Software Solution for Single Cell Genomics
Laboratory Informatics Weekly Update – Volume 14, Issue 32
August 10, 2016 Laboratory Informatics Weekly Update Volume 14, Issue 32 In This Issue Webcast Focus AUGUST 17, 2016: WEBINAR - Maximizing LabVantage LIMS' Value and Minimizing Implementation Risks In CSols’ experience, successful LabVantage LIMS implementations begin with a set of critical preparatory tasks. Organizations that complete these tasks are more successful and get more value out of their LIMS. Event Focus SEPTEMBER 26-30, 2016: 14th Cold Chain GDP & Temperature Management Logistics Global Forum The world’s largest event for temperature-controlled life science supply chains will return this year with extended topic focuses, session formats, speaking faculty and vendor options.…The challenges of data quality and data quality assessment in the big data era
While big data is a popular topic these days, the quality of that data is at times overlooked. This 2015 paper published in Data Science Journal attempts to address that importance and lay out a framework for big data quality assessment. After conducting a literature review on the topic, Cai and Zhu analyzed the challenges associated with ensuring quality of big data. "Poor data quality will lead to low data utilization efficiency and even bring serious decision-making mistakes," they conclude, presenting "a dynamic big data quality assessment process with a feedback mechanism, which has laid a good foundation for further study of the assessment model."
LabVantage and Lonza partner to offer the most advanced environmental monitoring capabilities in the industry
AUGUST 17, 2016: WEBINAR – Maximizing LabVantage LIMS’ Value and Minimizing Implementation Risks
AUGUST 17, 2016: WEBINAR – Maximizing LabVantage LIMS’ Value and Minimizing Implementation Risks
Sr. IT Validation Specialist – LIMS
Overview
Our client is seeking a Sr. IT Validation Specialist whose principal responsibilities include creating and reviewing the following for LIMS applications: SOP's, Validation Master Plans, Requirements and Risk Analysis, Traceability Matrix, IQ/OQ/PQ protocols and reports, Testing Documents and reports, Data Migration Plans and reports, Test Plans, Test Scripts, Discrepancy resolution
This 6-month W-2 contract is located in New Haven, CT
Skills and Qualifications:
- Bachelor’s Degree
- 3 – 6 years of relevant experience
- Excellent understanding of 21 CFR Part 11, ICH standards, EMEA, GLP, GCP, GMP, GDP regulations, GAMP Methodologies and general Software Development Standards.


