• The main changes driving adoption of regulatory technology in MedTech
• What the future regulatory landscape for MedTech will look like
• The relationship and importance between Regulatory Information Management (RIM), Regulatory Intelligence (RID), and Quality Management (QMS) data and processes

Learn what to look for in a RIM for MedTech solution and how to optimize your regulatory processes. Hear from a leading medical device company on how they solved their key challenges. Ask the experts your important questions.

MODERATOR

Philip Johnson
Sr. Principal, Quality and Compliance Solutions, IQVIA

KEY SPEAKERS

Robert Killpack
QA Applications Manager, Dentsply Sirona

Karl Nittinger
Director of Corporate Regulatory Affairs, Dentsply Sirona

Caroline Freeman
Senior Consultant, Quality Compliance Solutions, IQVIA

Carl Hackett
Director, Regulatory Technology Solutions, IQVIA

Jens-Olaf Vanggaard
Director, Global Regulatory and Safety Solutions, IQVIA