RQM+ is a global MedTech service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for Med Device and IVD companies, from concept to commercialization to post-market.

Our portfolio of services enables the delivery of end-to-end solutions across the complete med device product lifecycle, with our: 
• Regulatory and Quality Consulting
• Lab Services (Jordi Labs)
• Clinical Trials
• Reimbursement
• Technology Solutions


RQM+

Manufacturers often focus on MDR or IVDR and miss cross-cutting EU laws that impact CE marking, technical documentation, quality systems, and reporting. As a result, devices may be delayed, blocked from the market, or recalled, and manufacturers may suffer legal penalties and reputational harm. 

In this RQM+ Live! panel discussion, experts from BSI, Brabners, and RQM+ map how sectoral, horizontal, and national requirements fit together, how notified bodies assess them, and how to build an evidence-based path to EU market access. 

We will cover practical implications of recent and emerging regulations, including: 

*   Batteries Regulation (EU) 2023/1542 
*   AI Act (EU) 2024/1689 
*   Packaging and Packaging Waste Regulation (EU) 2025/40 
*   European Health Data Space Regulation (EU) 2025/327 

You’ll learn: 

*   How to identify all applicable legislation for your product and verify coverage. 
*   What notified bodies expect to see and the typical level of scrutiny. 
*   How to structure your compliance register, QMS updates, and regulatory reporting. 
*   Transition timelines and planning tactics to avoid last-minute surprises. 

Who should attend: Regulatory, quality, clinical, legal, and product leaders responsible for EU market access for medical devices and IVDs. 

Panelists and moderator: 

*   Greg Griffin, BSI 
*   Claire Burrows, Brabners 
*   Chris Parr, RQM+ 
*   Jaishankar Kutty, RQM+ 

A certificate of attendance is available upon request for live attendees.
