Events and webinars

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Replay
Navigating regulatory change: Why streamlined process management is critical for medtech regulatory teams
Navigating regulatory change: Why streamlined process management is critical for medtech regulatory teams
May 6-8
RAPS Euro Convergence
RAPS Euro Convergence
Replay
Post-EU MDR Compliance: Key Insights and Activities to Maintain Compliance after Device Certification
Post-EU MDR Compliance: Key Insights and Activities to Maintain Compliance after Device Certification
Replay
Taking SaMDs to market in the US
Taking SaMDs to market in the US
Replay
MDR & IVDR Lessons for Regulatory Strategy
MDR & IVDR Lessons for Regulatory Strategy
Replay
eSTAR submissions overview and live Q&A with FDA
eSTAR submissions overview and live Q&A with FDA
Replay
From planning to acceptance - navigating submissions strategy and FDA market pathways for medical devices
From planning to acceptance - navigating submissions strategy and FDA market pathways for medical devices
Replay
Regulatory AMA: EU MDR Transition Period Extension
Regulatory AMA: EU MDR Transition Period Extension
Replay
Optimizing Regulatory Communication
Optimizing Regulatory Communication
Replay
Quality & Regulatory Alignment for Audit Readiness
Quality & Regulatory Alignment for Audit Readiness
Replay
Regulatory strategy as a competitive advantage
Regulatory strategy as a competitive advantage
Replay
Exploring the gap between FDA and MDR risk management requirements
Exploring the gap between FDA and MDR risk management requirements
Replay
RAPS Ask an Expert: Everything you wanted to know about UDI
RAPS Ask an Expert: Everything you wanted to know about UDI
Replay
Insights and actions from the 2023 medtech regulatory performance report
Insights and actions from the 2023 medtech regulatory performance report
Replay
The Impact of MDR transition period extensions
The Impact of MDR transition period extensions
Replay
Medtech Post-market essentials
Medtech Post-market essentials
Replay
Regulatory clearance for medical devices
Regulatory clearance for medical devices
Replay
Regulatory Ask Us Anything: Medical Device submission strategy in China for imported devices
Regulatory Ask Us Anything: Medical Device submission strategy in China for imported devices
Replay
Actionable regulatory insights and process optimization for MDR/IVDR compliance
Actionable regulatory insights and process optimization for MDR/IVDR compliance
Replay
Why a regulatory information strategy is critical for successful MDR/IVDR transitions
Why a regulatory information strategy is critical for successful MDR/IVDR transitions
Replay
Regulatory AMA - What do you want to know about UDI?
Regulatory AMA - What do you want to know about UDI?
Replay
Introducing Rimsys 5
Introducing Rimsys 5
Replay
Why UDI is a regulatory concern - and not just an operational process
Why UDI is a regulatory concern - and not just an operational process
Replay
RIM for medical devices - challenges and opportunities for automation
RIM for medical devices - challenges and opportunities for automation
Replay
A medtech imperative: better regulatory information management
A medtech imperative: better regulatory information management
Replay
Integrate your regulatory stack for outsized results
Integrate your regulatory stack for outsized results
Replay
Modernizing medtech product registrations
Modernizing medtech product registrations
Replay
Global digital transformation for medtech regulatory affairs
Global digital transformation for medtech regulatory affairs
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