Events and webinars

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Dec 8
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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