Resource Library

Webinars

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