4th Annual Life Science Compliance Training Conference

June 2019 | Chicago, IL
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“I thought the conference was excellent!  Having a conference tailored to one discipline made each panel and contact relevant.”

Director, Compliance & Legal Affairs
Orexigen

“Great insight to hear payer perspective in contracting and account management and the changing healthcare landscape.”

Channel Liaison
Biogen

“It was definitely an excellent well-rounded opportunity to meet new people, get new ideas, and get an in-depth education on what’s to come with the FDA collaborations.”

Quality Engineer
Centurion Medical Products

“It was very well organized event and high quality, the fact to have an IVD track was also interesting. Thanks, I will recommend the Q1 event!”

Regulatory Affairs – EMEA Regional Head
BIOMERIEUX

“The organization and support staff were fantastic! I’m looking forward to next year.”

Global Business Project Lead
Genentech

About the Conference:

Pharmaceutical and Medical Device Corporations face continued pressure to ensure staff members in all functional areas are aligning business practices with evolving regulatory compliance frameworks, whether in commercial, research or operational roles. As information continues to become more accessible for employees through pervasive access to technology, compliance trainers must ensure staff fully comprehend the regulations surrounding the use and disclosure of information. For compliance trainers, pushing the limits of traditional training is of essential importance, to ensure staff members truly understand the legal ramifications of actions, to ensure information is retained, as well as ensuring training content and delivery is truly effective.

Topics to Be Addressed:

  • Interpreting Ongoing Areas of Legal Compliance Concern:
    • Foreign Corrupt Practices Act
    • Stark Law
    • Fraud & Abuse
  • Designing & Delivering Compliance Training for Executives
  • Impact of Monitoring vs. Measuring Compliance Data
  • Adapting Training Based on Perceived & Evaluated Risk

Program Highlights:

  • Comprehensive Participation from Pharma & Device
  • Legal Experts On-Site to Clarify and Interpret Laws
  • Interactive Sessions to Engage & Benchmark

Audience

75 Attendees

All attendees come directly from life science companies

Distinguished Presenters

Speaker recruitment in process

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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