- videocam Live Webinar with Live Q&A
- calendar_month June 9, 2026 @ 1:00 PM ET/10:00 AM PT
- signal_cellular_alt Intermediate
- card_travel Health
- schedule 90 minutes
Healthcare Under the Second Trump Administration: Regulatory Updates, Trends, Client Advisory Strategies
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About the Course
Introduction
This CLE webinar will examine the impact that the first year of the second Trump administration has had on healthcare regulation and the legislative agenda. The panel will examine the administration's policymaking priorities, regulatory changes, how the states have responded, and what may continue to be expected from agency leadership and rulemaking moving forward.
Description
Healthcare regulation and policy have rapidly evolved over the past year during the second Trump administration. Key changes include narrowing ACA marketplace access, imposing Medicaid work requirements, limiting access to reproductive healthcare, targeting gender-affirming care and vaccines, and increasing drug pricing transparency.
More recently, the White House released the proposed framework, The Great Healthcare Plan, aimed at lowering insurance premiums and prescription drug costs as well as reducing the influence of pharmacy benefit managers.
Listen as our expert panel provides healthcare counsel with an update on the significant regulatory changes made to date in the healthcare arena during the second Trump administration. The panel will discuss what policy and regulatory changes may still be on the horizon and address strategies for helping clients navigate this evolving regulatory landscape.
Presented By
Ms. Johnson focuses her practice on matters primarily for clients in the healthcare industry. She provides regulatory and compliance assistance on both a federal and state level. Ms. Johnson has assisted clinical laboratories, hospitals, long-term acute care hospitals, community hospitals, physician specialty groups, telehealth providers, surgery centers, healthcare associations, pharmacies, and other healthcare providers on regulatory, licensing, compliance, reimbursement, contractual, and corporate matters. She has provided support to entities during licensure and accreditation surveys and assisted in navigating state professional licensure laws, CLIA standards and state and federal laboratory laws and regulations, government and private payor reimbursement, state and federal fraud and abuse rules, state telehealth laws, and state and federal pharmacy regulation. Ms. Johnson also has advised clients on direct-to-consumer testing issues and applicable state requirements.
Ms. Klein advises businesses on assessing and mitigating risks related to the privacy and security of personal data, ownership, and commercialization of data AI; planning, drafting, and implementing privacy, security, and data protection policies and “best practices”; compliance with global, federal, and state privacy and security laws, regulations, and rules; data governance; and breach response, crisis management, and remedies for noncompliance. She has deep experience in negotiating and drafting complex technology and cloud transactions, licensing, and strategic IT and commercial agreements. Ms. Klein is a member of an HHS task force that is addressing aligning healthcare industry security approaches to responding to cybersecurity threats under the Cybersecurity Information Sharing Act of 2015. She also is a commissioner of the Electronic Healthcare Network Accreditation Commission, a voluntary, self-governing standards development organization established to develop standard criteria and accredit organizations that electronically exchange health care data. She is the former associate general counsel at Siemens Medical Solutions USA where she notably focused on operationalizing healthcare and life science regulations, including HIPAA/HITECH and the Common Rule in research.
Ms. Papish concentrates her practice on matters involving healthcare fraud and abuse and white-collar defense. Notably, she has significant experience working on a range of high-stakes, complex civil and commercial litigation matters and government and internal investigations. Ms. Papish regularly represents clients in False Claims Act litigation and related civil and criminal investigations by the U.S. DOJ, HHS-OIG, FDA, DEA, and other federal and state regulators. Her work is concentrated on the healthcare and life sciences industries but has spanned a number of others, including technology and financial services.
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This 90-minute webinar is eligible in most states for 1.5 CLE credits.
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Live Online
On Demand
Date + Time
- event
Tuesday, June 9, 2026
- schedule
1:00 PM ET/10:00 AM PT
I. Introduction
II. Key regulatory and policy changes made during the first year of the Trump administration
A. ACA
B. Medicaid
C. Prescription drug prices
D. Vaccines
E. Gender affirming care
F. Reproductive care
G. Others
III. State responses
IV. Trends moving forward
A. The Great Healthcare Plan
V. Best practices for helping clients navigate evolving regulatory landscape
The panel will review these and other important considerations:
- What key healthcare regulatory and policy changes occurred during the first year of the second Trump administration? What does the healthcare regulatory landscape potentially look like moving forward?
- What have the states been doing to align with or counter the federal initiatives, and what is the effect on healthcare clients?
- What strategies may be helpful when guiding clients through this changing legal landscape?
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Healthcare Under the Second Trump Administration: Regulatory Updates, Trends, Client Advisory Strategies
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