| Web: | mayocliniclabs.com |
|---|---|
| Email: | mcl@mayo.edu |
| Telephone: | 800-533-1710 |
| International: | +1 855-379-3115 |
| Values are valid only on day of printing | |
| Web: | mayocliniclabs.com |
|---|---|
| Email: | mcl@mayo.edu |
| Telephone: | 800-533-1710 |
| International: | +1 855-379-3115 |
| Values are valid only on day of printing | |
PACE / State of FL
This “Continual Improvement” webinar will provide an overview of new or changed regulations for 2022, and other regulatory issues that have the potential to affect clinical laboratories. The latter half of the year has been very busy for laboratory-related regulations and legislation, including the potential VALID Act and its impact to laboratory developed tests (LDTs), the SALSA Act which seeks to address reimbursement issues with the Protecting Access to Medicare Act (PAMA), and the potential end of the COVID-19 public health emergency.
R. Ross Reichard, M.D., DLMP Vice Chair of Quality and Associate Chair of Practice, recently contributed to a College of American Pathologists (CAP) article in CAP Today. The article, "How the Laboratory Drives Patient Satisfaction," explores the myriad ways laboratories can monitor and improve the patient experience.