Webinar: EXTEDO Customer Success Series: ​ REIG JOFRE’s Path to IDMP Readiness

With the clock ticking on IDMP compliance, regulatory teams everywhere are asking themselves: Are we truly ready?

For Laboratorio Reig Jofre, this question became the catalyst for change. Facing tight timelines and complex requirements, their regulatory professionals knew that relying on manual processes and scattered information would put compliance and efficiency at risk. The decision was made: it was time to set up a system that could manage medicinal product registration data in compliance with XEVMPD and IDMP. They found the right solution in EXTEDO's Registration Management Hub powered by CARA. 

We are delighted to welcome Noemi Fernández, Regulatory Affairs Specialist at Laboratorio Reig Jofre, who joins us in this session. She will share her firsthand experience: from navigating initial uncertainty, through the decision-making process, to the moment their new system went live. Together with Puneet Kaushik, Business Consultant at EXTEDO, she will walk you through the entire journey:

Date: 16 April 2026
Time: 15:00 – 16:00 CEST / 10:00 – 11:00 EDT

Use the opportunity and register now to hear directly from someone who faced the same challenges as your organization, overcame the same doubts, and built a solution that now drives their compliance and efficiency every day.

Hear more from Noemi and Puneet about the following topics:

• Preparing for Tomorrow – Why RIM was the strategic choice to meet IDMP requirements
• Finding the Perfect Fit – How Reig Jofre chose EXTEDO as their trusted partner
• Stronger Together – Laying the groundwork for success
• A Structured Journey to Compliance – From kick-off to go-live
• Empowered for the Future – Compliance, confidence, and efficiency

Your Speakers:

	Noemi Fernández Regulatory Affairs Specialist Laboratorio Reig Jofre
	Puneet Kaushik Business Consultant EXTEDO