What’s New In Quality and Regulatory? (2026)

Tuesday, Oct. 13, 2026
11 a.m.–Noon CT

Cost

Free for all participants.

Overview

This webinar reviews key federal legislative and regulatory developments affecting clinical laboratories, including PAMA reimbursement reform, the Enhancing CLIA Act, the CLIA modernization RFI, termination of COVID-19 EUA authorities, and recent CLIA memo updates.  

Presenters

Chelsea Conn, M.A., CQA(ASQ), MLS(ASCP)CM  

Director of Regulatory Affairs
Department of Laboratory Medicine and Pathology
Mayo Clinic, Rochester, Minnesota 

Jennifer Nosbisch, MBA 

CLIA Compliance Program Manager 
Revenue Compliance Office, Integrity and Compliance Office 
Mayo Clinic, Rochester, Minnesota 

Learning objectives

Upon completion of this activity, participants should be able to:

  • Summarize the current status of PAMA and Medicare laboratory reimbursement reforms. 
  • Describe the proposed Enhancing CLIA Act and its potential impact on LDT oversight. 
  • Explain the purpose and major themes of the 2026 CLIA RFI. 
  • Discuss the implications of HHS terminating COVID-19 EUA declarations. 
  • Identify operational and compliance impacts arising from recent CLIA memo updates. 

Intended audience

This webinar is appropriate for laboratory administrators and managers, safety coordinators, quality assurance and control staff, supervisors, and other laboratory personnel who are dedicated to safety, continuous quality, and process improvement. 

Credit

The following types of credit are offered for this event:

ASCLS P.A.C.E.®

Mayo Clinic Laboratories is approved as a provider of continuing education programs in the Clinical Laboratory Sciences by the ASCLS P.A.C.E.® program. This program has been approved for a maximum of 1.0 P.A.C.E.® contact hour.

State of Florida

Mayo Clinic Laboratories is approved as a Continuing Education Accrediting Agency for the Clinical Laboratory Sciences for the State of Florida. Florida Board of Clinical Laboratory Personnel has designated this program for General (Supervisor/Administration, Quality Control/Quality Assurance, and Safety) credit. This program has been approved for 1.0 contact hour.

To obtain credit


To obtain credit: 

  1. Watch the video.
  2. Complete the posttest and evaluation that launches immediately following the video. 
  3. Generate and print your certificate.  

Level of instruction for this program is basic.


Faculty disclosure


Course director(s), planning committee, faculty, and all others who are in a position to control the content of this educational activity are required to disclose all relevant financial relationships with any commercial interest related to the subject matter of the educational activity. Safeguards against commercial bias have been put in place. Faculty members also will disclose any off-label and/or investigational use of pharmaceuticals or instruments discussed in their presentations. Disclosure of this information will be published in course materials so those participants in the activity may formulate their own judgments regarding the presentations.

Questions

Contact us: mcleducation@mayo.edu

MCL Education

This post was developed by our Education and Technical Publications Team.