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Fulbright & Jaworski L.L.P.

Benjamin Koplin, Ben Koplin, Koplin, Fulbright & Jaworski L.L.P., Fulbright & Jaworski, Fulbright and Jaworski, Fulbright, health care, health law, health, Austin, COBRA, HIPAA, STARK, FCA, False Claims, AKS, Medicaid, Medicare, Anti-kickback, antikicback, labelling, certificate of free sale, CFS, fraud, investigation, internal, medical equipment, DMEPOS, medical device, fantastic, competitive bidding program, supplier, medicare, provider, fcpa, false claims act, foriegn corrupt practices act
Benjamin Koplin - Fulbright & Jaworski LLP
Benjamin Koplin
Senior Associate
D: +1 512 536 2439
Austin
98 San Jacinto Boulevard
Suite 1100
Austin, TX 78701-4255
T: +1 512 474 5201
F: +1 512 536 4598
AREAS OF CONCENTRATION
EXPERIENCE

Senior Associate Benjamin Koplin practices in the firm's Austin office. He focuses primarily on health care compliance and the federal regulation of health care providers and suppliers through agency actions, the Anti-Kickback Statute, the Stark Law, state and federal false claims acts, and the privacy and security of health information (HIPAA), as well as assisting in design and implementation of corporate compliance programs and various transactional matters involving health care entities.

REPRESENTATIVE EXPERIENCE
  • Development and implementation of global health care compliance programs for multiple life sciences companies including medical device manufacturers, genetic testing manufacturers and labs, clinical laboratories and durable medical equipment manufacturer/suppliers
  • Audit, benchmarking and revision of global health care compliance programs in the life sciences industry including revision of program documents (policies/procedures/work instructions/contracts/sales forms), sales and business unit leadership training, and assistance with ongoing monitoring and audit activities
  • Assists life sciences manufacturers, sales organizations and distributors in complying with various transparency laws and regulations, including state laws and the federal Sunshine Act
  • Advises life sciences companies on FDA labeling/recall issues, human subjects research protections and clinical trial issues
  • Representation of device manufacturer in grand jury investigation and civil litigation regarding business practices
  • Advised national DME manufacturer and supplier regarding competitive bidding issues
  • Representation of national retail pharmacy chain in coordinated federal and state investigations of dispensing practices affecting Medicaid claims
  • Representation of pharmaceutical wholesalers in National Medicaid Fraud Task Force and Texas Attorney General investigations regarding Medicaid rebates and in compliance issues related to drug pedigree rules
  • Assisted clients with creation, implementation, assessment, benchmarking and improvement of comprehensive corporate compliance programs including for international medical device manufacturers, DMEPOS suppliers and clinical laboratories to address compliance issues related to, among other topics, the Foreign Corrupt Practices Act, FDA regulatory issues, CLIA certification, Medicare billing practices, clinical research and product development, consultant and vendor relationships, product marketing and education and training activities
  • Advised DMEPOS suppliers and drafted memoranda and white papers related to business and legal risks and ramifications of participating in Medicare DMEPOS Competitive Bidding Program, assisted in design of supplier business models regarding same
  • Advised life science companies and health care providers on transactions, including on issues relating to federal Medicare anti-fraud and abuse, Texas illegal remuneration laws, the federal Stark law and Anti-Kickback statutes, and FDA regulatory issues
  • Prepared memoranda analyzing various hospital-physician arrangements for compliance with federal laws and regulations including the Stark Law and the Anti-Kickback Statute
  • Assisted with various transactional matters involving formation of nurse practices, rental and purchase of durable medical equipment, distribution of drug products, obtaining certificates of free sale, participation in Medicare durable medical equipment completive bidding process, analysis and guidance regarding researcher and physician-consultant arrangements, analysis of nutritional supplement labels, many of which included the preparation of purchase, employment and service contracts
  • Prepared and analyzed charity care and bad debt policies for compliance with Federal and State law relating to non-profit designation for Hospitals, especially in context of indigent-care lawsuits against hospitals
  • Briefed hospital clients on patient, facility and records access rights granted under federal law to Protection & Advocacy Systems, advised on strategy of addressing such Systems' requests for access
  • In self-disclosure context, internal investigations and qui tam suits against hospitals for billing and false claims allegations, analyzed documents such as physician recruitment agreements, lease agreements and compliance program policies and procedures for compliance with federal and state laws and rules
  • Developed comprehensive guidelines on hospital licensing for newly-constructed hospitals, including all ancillary licenses a hospital may need to secure
  • Analyzed documents and interviewed personnel at hospital clinic for violations of state pharmacy and medical board rules and laws and federal drug law, briefed issues and assisted in advising client on self-disclosure and employee relations options
  • Participated in two-year-long government investigation of and qui tam suit against international pharmaceutical company relating to off-label marketing and kickbacks to physicians, including full briefing of all issues of liability and arguments relating to propriety of company's actions; directed and oversaw review team of 26 attorneys for document review of over 2 million pages of documents relevant to requests for production
  • Briefed state and federal false claims and pharmaceutical issues and prescribing data related to multi-state investigation of pharmacy chain for alleged improper switching of drug dosage forms; assisted client in qui tam relator's fee recovery claims in the same suit
  • Prepared white paper to multi-state Medicaid Fraud Task Force analyzing and explaining drug repacker's responsibilities under the Medicaid Drug Rebate Program
PROFESSIONAL ACTIVITIES and MEMBERSHIPS
  • State Bar of Texas, Health Law Section
PUBLICATIONS
  • Co-author, "The Other Side of the Sunshine Act: Reporting Ownership & Investment Interests," Sunshine Forecast, March 21, 2013
  • Co-author, "Reporting ‘Indirect Payments’ Under the Sunshine Act: A Closer Look," Sunshine Act Forecast, March 4, 2013
  • Co-author, "Tracking Payments: How Should Manufacturers Allocate Food and Beverages?," Sunshine Act Forecast, February 13, 2013
  • Co-author, "Highlights of the Sunshine Act’s Final Rule
    Part 1: Key Changes and Clarifications," Sunshine Act Forecast, February 4, 2013
  • Co-author, "Final Rule Released for the Sunshine Act," Sunshine Alert, February 1, 2013
  • Co-author, "Still No Sunshine," Sunshine Forecast, January 11, 2013
  • "GAO Director of Health Care Kathleen King Testifies Regarding CMS Efforts to Reduce Health Care Fraud," Washington Health Care Update, December 4, 2012
  • "Department Of Health And Human Services Submits Sunshine Act Rules to OMB for Review," Washington Health Care Update, December 3, 2012
  • Co-author, "Department Of Health And Human Services Submits Sunshine Act Rules to OMB for Review," "Sunshine" Alert, November 30, 2012
  • Co-author, "Massachusetts Posts Final Rules on ‘Modest Meals’ and Reporting Requirements," "Sunshine" Forecast, November 29, 2012
  • Co-author, "Massachusetts Holds Hearing on Rules that Remove Reporting Requirements," Washington Health Care Update, October 25, 2012
  • "Texas Finalizes Medicaid Program Integrity Rules, Including Rules Governing Provider Compliance Programs," Washington Health Care Update, October 5, 2012
  • Co-author, "Massachusetts Proposed Rules Appear to Remove Reporting Requirements," Fulbright Alert, September 21, 2012
  • Co-author, "Boston Globe Reports Emergency Regulations Published Regarding Meals to Massachusetts Health Care Providers," Fulbright Alert, September 20, 2012
SPEECHES
  • Panelist, "Compliance: Current Investigative Initiatives," Fulbright & Jaworski L.L.P. Eighth Annual Health Law Symposium, Austin, TX, February 2-3, 2012
  • Co-presenter, "Governance Issues and the Role of the Compliance Officer" and "Overpayments Part 2: Stark Issues," Legal Issues Boot Camp for Compliance Professionals, Houston, TX, June 7-8, 2011
  • "Health Care Reform: An Overview of the 2010 Patient Protection & Affordable Care Act," Paychex CPA Educational Conference, July 29, 2010
EDUCATIONAL BACKGROUND

2006 - J.D., Harvard University Law School
2003 - B.A., magna cum laude, Boston University

While at Boston University, Ben was awarded the prestigious Warren O. Ault Prize for Outstanding Academic Achievement in History. He was admitted to practice law in Texas in 2006.

INTERESTS

As a former Division I crew bowman, Ben enjoys cycling, rock climbing, rowing and spending time with his family.

BAR AND COURT ADMISSIONS
  • Texas
CIVIC INVOLVEMENT






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