Webinars

Navigating regulatory change: Why streamlined process management is critical for medtech regulatory teams

Post-EU MDR Compliance: Key Insights and Activities to Maintain Compliance after Device Certification

Taking SaMDs to market in the US

MDR & IVDR Lessons for Regulatory Strategy

eSTAR submissions overview and live Q&A with FDA

From planning to acceptance - navigating submissions strategy and FDA market pathways for medical devices

Regulatory AMA: EU MDR Transition Period Extension

Optimizing Regulatory Communication

Quality & Regulatory Alignment for Audit Readiness

Regulatory strategy as a competitive advantage

RAPS Ask an Expert: Everything you wanted to know about UDI

Exploring the gap between FDA and MDR risk management requirements

Insights and actions from the 2023 medtech regulatory performance report

The Impact of MDR transition period extensions

Medtech Post-market essentials

Regulatory clearance for medical devices

Regulatory Ask Us Anything: Medical Device submission strategy in China for imported devices

Actionable regulatory insights and process optimization for MDR/IVDR compliance

Regulatory AMA - What do you want to know about UDI?

Why a regulatory information strategy is critical for successful MDR/IVDR transitions

Introducing Rimsys 5

Why UDI is a regulatory concern - and not just an operational process

RIM for medical devices - challenges and opportunities for automation

Modernizing medtech product registrations

A medtech imperative: better regulatory information management

Integrate your regulatory stack for outsized results

Global digital transformation for medtech regulatory affairs