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The past year has seen numerous challenges for medical labs, including the FDA’s final rule regulating laboratory developed tests (LDTs), as well as an increasingly difficult reimbursement environment, the usual uncertainty around PAMA, and other long-running issues.
How can lab managers and leaders, including those in hospitals, freestanding clinics, physician offices, and pathology labs, stay on top of these challenges and ensure smooth operations and profitability while avoiding compliance issues What other obstacles could be on the horizon and how can lab leaders best prepare for them? G2 Intelligence’s virtual Lab Institute event on November 12-13, 2024 will address these and other concerns.
This free two-day digital event will feature industry experts who will provide timely, accurate analysis of legal and regulatory issues, enforcement trends, and other developments that directly affect labs and other healthcare providers. Receive expert advice and guidance to help improve your lab’s operational performance and stay abreast of key industry trends. Following each presentation, there will be a Q&A session with these industry experts, and all the presentations will be available for free on-demand viewing after the live Lab Institute virtual event.
Key Topics Will Include:
- Laboratory Operations
- Compliance
- Regulations
- Legislation
- Enforcement Trends
- Reimbursement
- Technology
Note: You only need to register once to be signed up for all of the November 2024 Lab Institute talks.
Our Speakers:
Principal and Founder
Penn Avenue Law & Policy
Partner
Alston & Bird
Laboratory Director
Geisinger Medical Center
Member; Chair, National Healthcare Practice Group
McDonald Hopkins LLC
Member
McDonald Hopkins LLC
Member
Bass, Berry & Sims PLC
Member
Bass, Berry & Sims PLC
Director of Coding and Billing
BioReference
Director of Regulatory Affairs, Department of Laboratory Medicine and Pathology
Mayo Clinic
Principal
Carrot Clinical
Founder & CEO
Goldbug Strategies LLC
Agenda*
| Day | Time | Presentation Title | Speaker |
| November 12 | 11:00 AM – 12:00 PM ET | FDA’s Quality Management System Regulation: What Laboratories Need to Know | Christine P. Bump |
| November 12 | 12:30 PM – 1:30 PM ET | Lab Workflow Optimization: What to Consider Before You Start | Elsie Yu |
| November 12 | 2:00 PM – 3:00 PM ET | HIPAA Considerations for AI and Digital Pathology | Emily Johnson and Elizabeth Sullivan |
| November 13 | 11:00 AM – 12:00 PM ET | Washington Update: What Labs Should Know | Joyce Gresko |
| November 13 | 12:30 PM – 1:30 PM ET | Revenue Integrity: Understanding NCCI Policy and Application of the Rules | Robin Zweifel |
| November 13 | 2:00 PM – 3:00 PM ET | Lab Enforcement: Current Trends and Compliance Tips for Labs | Danielle M. Sloane and John C. Eason |
| November 13 | 3:30 PM – 4:00 PM ET | Panel Discussion: What’s Going on with LDTs Regulation? | Shannon Bennett, Julie Ballard, and Sheila Walcoff |
*Times, speakers, and presentation topics are subject to change.