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Articles & White Papers
Expert insights that explore and educate on best practices in laboratory informatics and digital quality & compliance.
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function instead. Please see Debugging in WordPress for more information. (This message was added in version 5.7.0.) in /home2/careersastrixinc/public_html/wp-includes/functions.php on line 5905The Integrated Lab - Article by Astrix for LabManager
White Paper - Data Governance Myths and a Foundation for Success
Bringing Clinical Development to a Successful Digital Transformation
Astrix Digital Transformation Podcast Series - Episode #2
Why Digital Transformations Fail: Cause & Recovery Program #2: January 2022
eBook - Guide to Validation 4.0 and the Digital Transformation of Quality
Transforming Supplier Quality Management in the Life Sciences Industry
Expert Insights Webinar Transcript
Strategies for leading a successful digital transformation in the lab
eBook - Bioinformatics - The digital future of life science research and development
White Paper - Transitioning from computer systems validation to computer systems assurance
Factors life science organizations need to consider
Scientific Computing World - A Digital Journey
Digital Transformation of Quality in the Life Science Industry
eBook - Why Strategic LIMS Program Management is Critical to the Success of your LIMS Deployment
8 Key Principles for a Successful LIMS Implementation
eBook - Harmonizing your Team in the Age of the Multigenerational Workforce
IntroductionMany companies are now employing a workforce that spans four different generations, each with its own unique values, motivations, perspectives, communication styles and work habits.
White Paper - Computer System Assurance – The Digital Era of FDA Compliance
Compliance for Digital Transformation Nearly a quarter of a century has passed since the U.S. Food and Drug Administration (FDA) established regulations on electronic records and electronic signatures, commonly known as 21 CFR Part 11, under which they are considered trustworthy, reliable and equivalent to the traditional paper records. The regulations provide guidance for organizations that maintain records or submit designated information electronically to the FDA, requiring computer system validation, audit trails, and record retention guidelines necessary for regulatory compliance.
Scientific Computing World
Article excerpt from SCW on Intelligent Integration in Laboratory Informatics - Full issue and article included here
Moving your Lab Software to the Cloud
In the quest to attain the digitally connected laboratory of the future, organizations are faced with seemingly insurmountable decisions regarding the scope and strategy that should be deployed to achieve this endeavor. Many organizations have advanced down one path or another towards digital transformation, only to encounter roadblocks along the way. Read More.
Building a Resilient Organization through Innovation and Agile Thought Leadership
Overview - The Covid-19 crisis has resulted in widespread disruption of our way of life, in both the home and workplace. Social distancing measures continue to impact everyday activities and businesses are faced with the dilemma of how to keep their workforce safe yet productive during these unprecedented times.
Industry Article - Navigating the Digital Journey
Dale Curtis and Bridgette Chambers discuss achieving digital transformation in the scientific laboratory
Transforming the Laboratory
Read the new article from Astrix on Scientific Computing World on the digitization of the modern laboratory
How to Reduce IT Risk in Lab Informatics Projects
Explore this informative white paper that provides an in-depth blueprint on how to research, select and implement laboratory informatics software in manner that reduces traditional IT project risk factors such as scope creep and cost overruns.
Data Integrity in FDA Regulated Labs
Verification of data integrity is a critical part of the FDA’s mission to ensure the safety, efficacy and quality of human and veterinary drugs, biological products, and medical devices. Read More