Events and webinars

Informa MedTech Summit

MedTech Regulatory Intelligence Summit

RAPS Euro Convergence

Rimsys RegUp Amsterdam

Regulatory strategy as a competitive advantage

Conquest: ComplianceQuest User Conference

Exploring the gap between FDA and MDR risk management requirements

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

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

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

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

Introducing Rimsys 5

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

RIM for medical devices - challenges and opportunities for automation

A medtech imperative: better regulatory information management

Integrate your regulatory stack for outsized results

Modernizing medtech product registrations

Global digital transformation for medtech regulatory affairs