Analysis of the Proposed Sunshine Rule: Legal Considerations

Slides:



Advertisements
Similar presentations
4.02 Compliance Training Brian A. Dahl Senior Counsel Takeda Pharmaceuticals North America, Inc. November 14, 2003.
Advertisements

H OGAN & H ARTSON, L.L.P.
PwC Medical Device Compliance Survey Discussion of Survey Results.
VCOM Conflict of Interest Policy Overview of Financial Conflict of Interest Related to Research December 4, 2013.
Code of Ethics for Professional Accountants
Conflict of Interest (COI) Objectives: Provide an overview of financial conflict of interest (FCOI) related to research activities at Gillette Describe.
Summary of NEPA and SEPA Coastal Engineering and Land Use Issues in North Carolina Greenville, NC January 13, 2009 Sean M. Sullivan.
Course on Professionalism ASOP 43 – Property / Casualty Unpaid Claim Estimates.
Health Insurance Portability Accountability Act of 1996 HIPAA for Researchers: IRB Related Issues HSC USC IRB.
O PEN P AYMENTS An Explanation of Section 6002 of the Affordable Care Act Center for Program Integrity September, 2013 CMS Disclaimer: This information.
Overview of Eligibility & Enrollment II Final Rule – Medicaid and CHIP Jennifer Ryan Center for Medicaid & CHIP Services July 17, 2013.
MSRB Proposed Rules and Interpretations NALHFA 2011 Annual Educational Conference May 20, 2011.
August 10, 2001 NESNIP PRIVACY WORKGROUP HIPAA’s Minimum Necessary Standard Presented by: Mildred L. Johnson, J.D.
The Advisers Act Custody Rule
1 Physician-Industry Transparency: The U.S. Physician Payment Sunshine Act.
Congress and Contractor Personal Conflicts of Interest May 21, 2008 Jon Etherton Etherton and Associates, Inc.
Cefic model SIEF Agreement: benefits and practical aspects CEFIC Legal Aspects of REACH Issue Team (LARIT) June 2009.
What options do states have? What is Georgia planning to do? What are some of the other states doing? What are the possible implications to permit fees?
Circular A-110 Everything You Didn’t Want to Know.
The Third Annual Medical Device Regulatory, Reimbursement and Compliance Congress Compliance Best Practices in a Post Orthopedic Environment David Matyas.
# Operating Under the New Compliance Environment: Considerations for the Pharmaceutical Industry The Impact of the new Medicare Prescription Drug benefit.
Confidentiality, Patient Safety Work Product, and PSOs The Proposed Rule Implementing the Patient Safety and Quality Improvement Act of 2005 AHRQ Annual.
Voluntary Codes MassMEDIC Meeting Are You Ready to Comply with Massachusetts’ New Pharmaceutical and Medical Device Code of Conduct Law? Linda D. Bentley,
© 2008 Foley Hoag LLP. All Rights Reserved. 1 The New Massachusetts Pharmaceutical & Medical Device Marketing Regulations How to Address and Overcome Likely.
1 Colorado Bar Association Health Law Section April 20, 2013 CMS Physician Payment Sunshine Act Final Rule: Sunshine or Black Hole? Michael M. Schmidt.
Pitfalls and Lessons Learned: Advanced Implementation Strategies for a Compliant Grant Process National CME Audioconference December 9, 2008.
Coding Compliance Plan July 12, Benefits of a compliance program  To demonstrate our commitment to honest and responsible conduct, decrease the.
Patient Protection and Affordable Care Act March 23, 2010.
Financial Interests1995 Regulations 2011 Final Rule Significant Financial Interests (SFI) threshold De minimis $10,000 for disclosure generally applies.
ABR224 Lecture 3 EEA. DUTIES OF DESIGNATED EMPLOYER [Sect. 13]  1) Consultation with Employees:  In order to ensure consensus regarding the implementation.
Lecture 4. OUTCOMES What must the equity plan include?. What must affirmative action measures include? Which factors are taken into account in determining.
H I P A A T R A I N I N G Self Directed Module 7 Research Disclosures For Data Custodians START Click to begin…
FleetBoston Financial HIPAA Privacy Compliance Agnes Bundy Scanlan Managing Director and Chief Privacy Officer FleetBoston Financial.
Fight On Training on NIH Conflict of Interest Rule and Introduction to diSClose Dan Shapiro Director, Research Compliance Ben Bell Manager, Research Compliance.
Faculty Council on Research April 11, 2012 Jeff Cheek, Ph.D. UW Associate Vice Provost for Research Compliance and Operations New PHS regulations on financial.
Partners Conflict of Interest Policy and Reporting October 11, 2012.
© 2004 Moses & Singer LLP HIPAA and Patient Privacy Issues Raised by the New Medicare Prescription Drug Program National Medicare Prescription Drug Congress.
Flowers Hospital General Compliance Training-Students 2013.
HIPAA Privacy Rule Positive Changes Affecting Hospitals’ Implementation of the Rule.
A risk assessment is the process of identifying potential hazards an organization may face and analyzing methods of response if exposure occurs.
Subject Injury at OHSU Darlene Kitterman, Director, Investigator Support, OCTRI Kathryn Schuff, MD, MCR, Chair, OHSU IRB Melanie Hawkins, RN, Director,
CIEBA Webinar DOL 2015 Fiduciary Proposal Jenny Eller Groom Law Group, Chartered May 20, 2015.
Improving Compliance with ISAs Presenters: Al Johnson & Pat Hayle.
Disclosure of Financial Interest Policy. Medical Staff Policy Approved by the MEC’s Aimed at protecting the integrity of the LMHS Medical Staffs Requires.
Chapter 4 The Legal and Regulatory Environment of Health Care.
HIPAA Privacy Rule Positive Changes Affecting Hospitals’ Implementation of the Rule Melinda Hatton -- Oct. 31, 2002.
Health Insurance Portability and Accountability Act of 1996
What is HIPAA? HIPAA stands for “Health Insurance Portability & Accountability Act” It was an Act of Congress passed into law in HEALTH INSURANCE.
The HIPAA Privacy Rule: Implications for Medical Research
Whistleblower Program
UCR PRO Reviewer Placemat
Compliance Program 2018.
VIth AIDA EUROPE CONFERENCE (Vienna, 3-4 November 2016)
Training Objectives What is the Signature Partners MSSP ACO?
Current Privacy Issues That May Affect Your Credit Union
The HIPAA Privacy Rule and Research
PSO Overview for (name of organization’s) PSES Workgroup
Accountable care organizations
Risk Management: why and how to protect your health center
Compliance of Voluntary Organisations
An Introduction to the Sunshine Act
Managing Federal grants
Safety and Regulatory Guidelines In the Medical Laboratory
PSO Overview for (name of organization’s) PSES Workgroup
Upcoming PIPEDA Changes
Compliance of Voluntary Organisations
Internal Control Internal control is the process designed and affected by owners, management, and other personnel. It is implemented to address business.
Implementing Controls Around Grants, Consulting Agreements, CME, Preceptorships, and Other Promotional Practices Paul E. Kalb Heidi C. Chen Fourth Annual.
POST-ISSUANCE COMPLIANCE
NIH Concerns over Foreign Influence
Presentation transcript:

Analysis of the Proposed Sunshine Rule: Legal Considerations Meenakshi Datta mdatta@sidley.com (312) 853-7169 January 11, 2012

Policy Overview Concern within Congress and among prosecutors and other enforcement officials regarding conflicts of interest and inappropriate influence Purposes of Sunshine Act disclosure include: Transparency and public awareness Discourage inappropriate conflicts of interest from developing CMS soliciting comments on the intricacies of the disclosure obligation and balancing the need to discourage inappropriate conflicts of interest without dissuading the development of beneficial arrangements

Potential Legal Issues Numerous proposals with significant legal implications, including: Delayed Reporting Definitions of Applicable Manufacturer and Common Ownership Reporting Educational Material Reporting Research Reporting Compensation for Speaking Arrangements Submission of Assumptions Letters Disputed Reports and Opportunity to Amend Previously Reported Data Potential for Sunshine Act reporting to create Federal Anti-Kickback and False Claims Act risks, among others, for manufacturers Sunshine Act reports provide a significant data mining opportunity for Congress and prosecutors Among the many challenges – compliance, operational, and implementation – will be designing and implementing safeguards to mitigate AKS, FCA, and other legal risks

Delayed Reporting CMS purports to delay the need to begin tracking payments until after the final rule is promulgated States that manufacturers may begin to collect information “voluntarily” Proposed 90-day “preparation period,” following the issuance of the final rule to afford manufacturers additional time to comply with the final rule’s data collection requirements Legal considerations: What is meant by CMS’ suggestion that manufacturers might voluntarily collect information? What are the implications for manufacturers who do so? Is the proposed preparatory period sufficient for the manufacturer to adjust its systems? What if the system isn’t ready following the conclusion of the preparatory period? Consider back-up plans to meet legal obligations

Definitions: Applicable Manufacturer and Common Ownership Expansive proposed definitions Applicable Manufacturer: Global reach: Physical location or country of incorporation is not relevant; what is relevant is whether the entity sells or distributes a covered product in the U.S. All payments: Applicable manufacturers must report all relevant payments, even on non-covered products so long as the manufacturer has at least one covered product Common Ownership: Proposal One (Broader): When the same person directly or indirectly owns any portion of two or more entities Proposal Two (Slightly Narrower): When the same person directly or indirectly owns 5% or more of two or more entities Intricate rules about under what circumstances entities under common ownership must report separately versus together Important legal implications for entities with global operations, brand and non-Rx products, and complex corporate structures

Reporting Educational Material Statute specifies an exception for “[e]ducational materials that directly benefit patients or are intended for patient use” The implication is that other educational materials that do not fall within another exception must be reported CMS states that the exception is limited to “materials’’ (including written and electronic materials), but excludes “services or other items” CMS solicits comment on whether educational materials provided to covered recipients (for example, a medical textbook) should be interpreted as educational materials that ‘‘directly benefit patients’’ Legal considerations include: Implications for education materials for covered recipients Examples: manufacturer-sponsored disease management or reimbursement information programs; reprints PhRMA and AdvaMed-Code compliant educational items to covered recipients

Reporting Research CMS solicits comments on the definition of “research” Should there be a separate category or categories for certain research activities such as post-marketing research, studies without research protocols, or studies not conducted pursuant to a written contract? Important proposal for delayed publication: Proposal One: delay publication of research payments to covered recipients for services in connection with research on, or development of new covered products, as well as new applications of existing covered products Proposal Two: limit delayed publication for those payments in connection with clinical investigations for new covered products only Reporting direct and indirect research payments; dual reporting for research payments to teaching hospitals; lump sum reporting for indirect research payments Considerations include data mining opportunities, disclosure of payments related to confidential clinical studies, and potential for consumer misinterpretation of payments subject to dual reporting and lump sum reporting

Reporting Compensation for Speaking Arrangements Sunshine Act requires that applicable manufacturers report direct compensation to physicians serving as speakers or faculty for a ‘‘medical education program” CMS proposes to broaden this requirement to reach any speaking arrangement e.g., dinner programs CMS is weighing creating a separate payment category for speaking arrangements that are outside the context of a medical education program Legal considerations include data mining opportunities if additional payment category is established and additional reporting obligations that are not specified in the statute

Submission of Assumption Letters CMS seeks comment on its proposal to permit applicable manufacturers to submit assumptions letters with their annual reporting form to describe the manufacturer’s practices with regard to categorizing the nature of the various payments and transfers of value it reports CMS also seeks comment on whether the submission of assumptions letters should be mandatory Legal considerations include: If assumptions are not mandatory, whether such assumptions should be documented at all, documented internally, or documented and submitted to CMS Potential enforcement risk mitigation tool Content of such assumptions (should they cover just the manufacturer’s practices with respect to categorizing payments, as specified under the proposed rule, or should they cover other issues as well such as operational or implementation limitations?)

Disputed Reports and Opportunity to Amend Previously Reported Data CMS seeks comment on its proposed dispute procedure Covered recipient’s understanding of the payment amount is what will be used by CMS to provide aggregated totals to the public CMS is also considering aggregating totals using the manufacturer’s understanding of the payment amount CMS also seeks comment on its procedure for manufacturers to amend previously reported data 45-day review period for then-current and prior reporting year Legal considerations include data mining based on disputed data and whether to report to CMS corrections to data that are identified following the close of the review period

Safeguards to Mitigate Legal Risks Developing robust tracking and reporting systems, with regular compliance audits and monitoring Establishing appropriate policies and procedures for “front end” reporting and “back end” data review and correction Implementing effective compliance training for affected personnel Consider: Analyzing payment trends prior to submission of reported payments to CMS Undertaking legal review of payment data prior to submission to CMS Documenting assumptions Submitting assumptions and any limitations on certification to the government

End