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 recently promoted to the Compliance group within my company and while I had an understanding of the business, there were areas where I needed some additional knowledge. My boss recommended this program as a great immersion into the world of compliance – and she was right! In the four-day U.S Healthcare Compliance Program, we covered topics from the Federal Anti-Kickback Law to Creating a Culture of Compliance, and worked through interactive case studies. The experience was great and the tools I left with allow me to review the material whenever I need. This program is great for both newer and experienced compliance professionals. With the ever-changing climate we work in, this program not only helps to keep you up-to-speed on changes to relevant laws and regulations, but also helps identify areas where your company could be at risk. Attending this program was a great investment in my professional development and has already proven to be a great investment to my company. "
Principal Compliance Specialist | Diabetes Group Office of Ethics and Compliance
- 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 firstname.lastname@example.org 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 email@example.com or call 973-642-8871.