June 11th, 1:00pm ET Significant cases decided in 2024 and 2025 are shaping the landscape of enforcement for clinical laboratories. Government regulators continue to focus on medical necessity and improper business relationships, but they have expanded their focus...
Key steps labs can take to avoid some of the most common data protection compliance issues related to emerging technologies, and add value
Regulatory experts will address key questions remaining about LDTs and how labs may wish to address compliance amidst the uncertainty
This webinar will provide an in-depth overview of the new QMSR requirements and outline key steps laboratories must take to ensure compliance
This session will offer an analysis of how instrument consolidations and total laboratory automation can improve lab workflow optimization
Learn how to translate NCCI policy statements into layman’s terms with working examples that can be applied within your organization
This Lab Institute presentation offers updates on recent legal and regulatory developments, and how they could affect labs
This Lab Institute presentation shares recent enforcement trends and how labs can avoid compliance risks related to these issues.
Our event equips diagnostic medicine professionals with innovative strategies to advance their practice, enhance patient care, and drive the future of the field
This webinar explains how Loper Bright could impact the laboratory industry and what it means for clinical lab operations
This webinar shares how the FDA's final rule applies to oncology LDTs and what it means for precision medicine efforts
This webinar will discuss steps lab leaders will need to take in the near future to ensure they are prepared for the final LDTs rule
