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Thought leadership, industry updates, and practical guidance for in-office laboratories.
Stay informed about best practices, regulatory developments, testing advances, and what's happening at Doc Lab.
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Preparing for National MolDx Adoption: What Labs Need to Do Now and How Doc Lab® Can Help
Molecular diagnostics are moving toward a more standardized, evidence-driven reimbursement environment. Here's what labs need to do now to align with MolDx requirements before it's too late.
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PCR Detects Pathogens Missed by Culture in 54% of Cases: Part III Research Reveals Critical Gaps in Traditional Testing
New research reveals conventional culture testing misses pathogens in 54% of complicated UTI cases—leading to a 50% treatment failure rate when resistance goes undetected. This Part III analysis shows why PCR-based diagnostics deliver better outcomes.
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510(k) vs De Novo FDA Pathways Guide 2025
Not sure whether your medical device needs a 510(k) or De Novo submission? This guide compares timelines, costs, and requirements to help you choose the right FDA pathway.
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FDA's LDT Rule Vacated: What This Means for Laboratory Diagnostics
A federal judge ruled the FDA cannot regulate LDTs as medical devices. Here's what laboratories need to know about this landmark decision and its implications for diagnostic testing.
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PCR Testing Outperforms Traditional Culture Methods for Complicated UTIs: New Research Findings
PCR testing outperformed traditional culture methods across every metric in a major two-part study on complicated UTIs—faster results, better detection, and improved patient outcomes.
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Revolutionizing Healthcare: The History and Benefits of Point of Care Diagnostics
Faster diagnoses, streamlined workflows, and cost savings—point-of-care diagnostics offer significant advantages for medical practices. We explore the history of POC testing and the benefits of bringing it in-house.
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