Partners Justin O'Brien and Greg Noonan presented a panel at the recent Medical Device & Legal Professionals: A Collaborative Exchange conference on December 11-12, 2014 in Washington, DC. Hosted with the Medical Device Manufacturers Association (MDMA), the conference brought together general counsel, private practice lawyers and medical device executives to discuss effective compliance programs, best practices and emerging trends in such areas as off-label marketing and mHealth, among others.
This program was called, "What to Do When Problems Arise" and focused on best practices in managing investigations, "dawn raid policies" and determining when to self-disclose issues.
The lively program was a must for medical device executives and those who are responsible for managing compliance programs and looking to increase their competency in managing internal investigations. This program was designed to assist medical device executives and their counsel, in a practical and hands-on manner, so that they may facie the many significant compliance threats of today and tomorrow with confidence.