PROGRAM SCHEDULE for 2017 TBD | San Francisco, California
This three-day educational program immerses attendees in the statutes, regulations, and other guidance that comprise the body of law known as "fraud and abuse law," as well as other healthcare-related laws and regulations, to help the audience understand the legal underpinnings of the life sciences compliance education programs they develop and enforce.
Who Should Attend
Professionals working for smaller pharmaceutical, biotech, medical device and diagnostics companies – particularly those working in a compliance, legal, regulatory or, medical affairs role. This program is also valuable for sales, marketing, grants and related areas, as well as outside counsel who represent life sciences companies and private equity and venture capital firms that fund these companies.
"I was fortunate to attend the Seton Hall Law European Healthcare Compliance Program after being nominated by our Senior Leadership Team. I enjoyed the program very much as it offered a comprehensive overview of health care laws and regulations, industry standards, and company practices. Even though I have been working in healthcare compliance for five years, many parts of the program were very new to me and the knowledge I gained has enabled me to perform my job more efficiently and effectively. Attending the program also provided me with the opportunity to hear many different perspectives and perceptions from program faculty and attendees alike. I would definitely recommend the program to other healthcare compliance professionals. "
Lead Specialist, Testing Operations; EMEA&Canada CoE – Global Operations
Johnson & Johnson, Health Care Compliance & Privacy
- Program faculty includes law professors, in-house compliance officers, high-level government, and private lawyers who are experts in pharmaceutical and medical device fraud and abuse issues.
- Session topics include Federal and State False Claims Acts, Federal Anti-Kickback Statute, the Food, Drug & Cosmetic Act (FDCA), Data Privacy (HIPAA, HITECH, and others), Food & Drug Administration Amendment Act of 2007 (FDAAA), International Anti-Corruption Laws, Prescription Drug Marketing Act of 1987 (PDMA), PhRMA Code and AdvaMed Code, the federal Sunshine Law, federal and state marketing and disclosure laws, OIG compliance guidance, and much more.
- Attendees receive extensive resource materials that will aid them in their ongoing compliance efforts.
- Attendees will receive a certificate issued by Seton Hall Law School upon completion of the Program, and may apply for NY and NJ CLE credit.
The Marker San Francisco
San Francisco, California
Cost & Registration
Tuition for the Program: $2,500. If you are a member of a life sciences trade organization, you may be eligible for a discount. Group discounts are also available. Please contact us at email@example.com or 973-642-8871 for more information. Register here.
To request more information regarding the Life Sciences Compliance Certification Program, please click here to submit a 'Request for Information' form. You may also contact us at firstname.lastname@example.org or call 973-642-8871.