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Resource Library

Webinars

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