Safety & Regulatory Compliance Predictions For 2025: Unlock Future Trends With IQVIA

Available On-Demand

Webinar

Join IQVIA to learn expert predictions from thought leaders on lifecycle safety, local pharmacovigilance, regulatory strategy, Medical Information (MI), and post-registration management for 2025.

Our panel of experts bring years of experience and deep insights into the evolving landscape of safety and regulatory compliance. Gain first-hand knowledge and specialized perspectives on the latest trends:

Uncover how health authorities are guiding the optimization of clinical trial recruitment, participation and dose optimization
Discover the essential strategies for navigating post-approval lifecycle management, MI and local pharmacovigilance
Explore the rapidly changing advances with Literature Services, Aggregate Reporting and Signal Management
Hear how artificial intelligence (AI) and machine learning (ML) technologies will be integrated into a combined safety services and technology model in 2025

Watch On-Demand Now! →

Meet the Speakers

Patrick Brady, PharmD

Global Head, Therapeutic Innovation & Regulatory Science, IQVIA

Ana Pedro Jesuíno

Associate Director, Marketed Product Safety, IQVIA

Simon Johns

Director, Medical Information & Marketed Product Safety, IQVIA

Marcela Miño

Global Head, Lifecycle Management & Regulatory Affairs, IQVIA

Sabika Rizvi

Director, Aggregate Reporting & Benefit-Risk Management Services, IQVIA

Watch on-demand now!

Work Email Address*

Role

Country*

Yes, I would like to be contacted by an IQVIA expert

I have read and agree to the below privacy policies

By ticking this box, you agree to receive emails from Citeline, and carefully selected partners

Lead Source - PI Partner

Primary Product Interest

By completing this form you agree Citeline and IQVIA may contact you directly about industry news, products, services and events that may be of interest to you subject to the privacy policies of Citeline and IQVIA.