Quality, Standards & Compliance
|3 min read
Laboratory Design Through the Micro-Meso-Macro Framework
Creating laboratory environments that prioritize scientific innovation and human well-being
|5 min read
What Latest EU 2024/1860 Amendment Means for IVD Manufacturers
Key deadlines and questions in vitro diagnostic manufacturers need to consider to comply with IVDR Amendment EU 2024/1860
|2 min read
'The Age of Artificial Intelligence'
The Today's Clinical Lab 2024 Genetics & Genomics print issue features insights on how to harness the power of genetics and genomics data analytics
|3 min read
Will President-Elect Donald Trump Change the FDA’s LDT Final Rule?
Clinical labs eager for relief from upcoming FDA compliance dates are looking to the new presidential administration
Updated |1 min read
Improve Analyzer Performance with Reliable Lab-Grade Water Solutions
Learn how a leading hospital biochemistry lab tackled water quality challenges to keep analyzers running smoothly and accuratelySponsored by
|2 min read
Experts Develop Laboratory Toolkit for Patients with Viral Hemorrhagic Fevers, Marburg Virus Disease
New resource provides guidance for healthcare facilities to perform basic laboratory testing in a safe and effective manner for patients at risk for viral hemorrhagic fevers
|2 min read
Initial Crowdfunding Assays Are Now Available in Response to LDT Final Rule
LISA heads up new effort with UTI assays designed to comply with the FDA’s regulations for lab-developed testsSponsored by
|2 min read
Understand Lab Equipment Performance Data for Smarter Decision-Making
Explore key performance metrics for refrigerators, freezers, and incubators to help ensure your lab operates efficiently and cost-effectivelySponsored by
|5+ min read
FDA, CLIA, and ISO—Which Regulations Apply to Your Clinical Lab?
Experts Julie Ballard and Lindsay Strotman help you navigate the complexities of FDA, CLIA, and ISO standards for the clinical lab
|1 min read
Stay Competitive in a Fast-Paced Environment by Addressing Key Operational Barriers
Implementing solutions to improve turnaround time, sample traceability, fragmented data, and regulatory issues can help labs better meet industry standardsSponsored by
|3 min read
First Ever Effort to Crowdfund Diagnostic Assays Launches in Response to FDA LDT Final Rule
LISA CEO explains why crowdfunding is a viable way to shoulder the new regulatory costs behind laboratory-developed testsSponsored by
|1 min read
Crowdfunding Solutions for CAP/COLA Labs to Overcome FDA LDT Rule Costs
Learn how clinical labs can leverage crowdfunding to reduce diagnostic test development costs and meet FDA LDT compliance requirementsSponsored by
