This webinar is now available OnDemand to view at anytime

Join experts from IQVIA for a discussion on:

  • Creating robust regulatory strategy across the entire drug development continuum
  • Maximizing early strategic advantages to enable operational efficiency
  • Enhancing regulatory affairs from pre-registration to post-registration
  • Using AI/ML and regulatory intelligence tools to lower administrative burdens
Watch OnDemand

Meet the Speakers

Michelle Gyzen

Sr. Director, Strategic Solutions, Reg. Affairs & Drug Dev. Solutions, IQVIA

Michel Denarié

Sr. Principal, Regulatory Affairs & Drug Development Solutions (RADDS), IQVIA

Successfully navigating constantly evolving regulatory matters across borders is a complex, time-consuming task. Learn tips for moving ahead in this important session.

Don’t miss key insights into improving your regulatory processes - watch now!

Our presenters will carry out a live Q&A, if you have any questions please let us know.
By ticking this box, you agree to receive emails such as relevant news, updates and offers from Informa Business Intelligence, and carefully selected similar products from our portfolio
By completing this form you agree IQVIA and Citeline may contact you directly about industry news, products, services and events that may be of interest. This is subject to IQVIA's privacy policy and Citeline’s privacy policy.