Forums & Workshops (Sep 11th) - EST/EDT (Eastern Daylight, GMT-4)
Successful medtech companies prioritize early planning, incorporating key milestones for regulatory compliance, market access, risk management, and stakeholder engagement. By doing so, they position themselves for growth and innovation in the dynamic healthcare landscape.
Join IQVIA's team of clinical development experts for a discussion on innovative pathways to bring your medtech product to market.
Agenda topics include:
• Regulatory Landscape: Explore current and emerging legislative and regulatory dynamics impacting your medtech products
• Evidence Generation: Prioritize planning for pre- and post-market evidence generation to facilitate smooth market entry
• Stakeholder Engagement: Learn how to effectively understand each stakeholder’s perspective and needs, including regulators, payers, and healthcare providers
• Innovative Case Studies: Share success stories that demonstrate strategies to de-risk medtech pathways, achieve regulatory approval, and optimize market access through data-driven differentiation