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Managed care and value-based reimbursement models are fast becoming the norm for payors and providers.  Please join us for a webinar discussing some of the key managed care contracting terms for brick-and-mortar and digital health services from the perspectives of a payor and a provider.  Topics will include what to look out for when preparing or reviewing a payor participation agreement, including unilateral amendments, prohibition against balance billing, incorporating provider manuals, credentialing standards, post-termination continuity of care services, and accessing and owning data.

Companies providing services to health insurers, self-funded health plans, and employers offering health benefits to employees should be aware of the potential need to obtain state licenses for certain activities.  Please join us for a webinar about state law licensing requirements and what it means to health plan service providers.  Topics will include the activities that may trigger licensing requirements, legal requirements for licenses, application requirements, and other related issues.

Top developments and predictions in the Life Sciences & Healthcare sector in China (CMS)
CMS
12 pages

Learn about top 2021 developments and 2022 predictions in the Life Sciences & Healthcare sector in China.

Resource Details
Interest Area: Health Law
Region: Asia, China
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Top developments and predictions in the TMT sector in China (CMS)
CMS
8 pages

Learn about top developments and predictions in the TMT sector (Technology, Media, and Telecom) in China.

Resource Details
Interest Area: Compliance and Ethics, Health Law, Government, Technology, Privacy, and eCommerce
Region: Asia, China
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On January 5th, the Federal Trade Commission (FTC) proposed a regulation that would ban virtually all forms of employee noncompete agreements across the country.  Please join us for a webinar about the FTC’s proposed rule and what it means for healthcare organizations.  Topics will include what the proposed rule would mean for mergers and acquisitions, whether it may apply to nonprofit organizations, and the potential for court challenges to the proposed rule.

Same same, but different. Using case studies we will discuss the FDA’s position on interchangeable biosimilars and what it means to be “highly similar” and have “no clinically meaningful differences”.

Description to come. 

ACC Colorado Presents

WEBINAR

Assessing Compliance Programs and Risks in a Volatile Environment

 

Wednesday, December 14, 2022
11 AM – 12PM MDT

CLICK HERE TO REGISTER

No Cost to Attend the Zoom Meeting

One CLE Credit Pending Approval

Please join Greenberg Traurig’s Cuneyt Akay in a discussion regarding U.S. Department of Justice guidance on evaluating corporate compliance programs, key sources of risk, program effectiveness data, and remediation of program weaknesses. In addition, he will address the legal violations that may hold people back from taking their businesses internationally, potential barriers limiting global expansion, and more trends related to the Foreign Corrupt Practices Act (FCPA).

Cuneyt A. Akay, Shareholder, Greenberg Traurig LLP, is an anti-corruption lawyer focused on helping clients comply with the Foreign Corrupt Practices Act (FCPA) and the UK Bribery Act. Cuneyt designs, builds, and implements effective compliance programs for clients around the world. Cuneyt’s experience includes conducting internal investigations, performing compliance risk assessments, handling pre-and post-acquisition compliance due diligence, training staff and third parties on compliance requirements, and assisting in the monitoring and auditing of anti-corruption programs. Cuneyt also represents clients in complex civil litigation, class actions, and appellate proceedings in both state and federal courts throughout the country. In addition, he advises clients on governmental matters, including election law issues, ballot initiatives, campaign finance, and administrative proceedings.

 

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