Netherlands Site

To serve your clinical supply needs within the European Union (EU), Xerimis NL offers Qualified Person (QP) services plus packaging, labeling, distribution, and storage in all temperature ranges. 

Our NL facility is a full-service facility in the Netherlands (Rozenburg). We’re proud to bring the highest level of service, flexibility, and responsiveness to your clinical trials, helping you reach patients in mainland Europe and anywhere else in the world.

 Xerimis NL Facility Highlights

  • Onsite QPs for batch release Certification and QP Declaration
  • Secondary packaging rooms
  • Cold-room packaging (refrigerated and frozen)
  • Controlled storage areas, alarm-monitored for all temperature ranges:

 

 

 

 

 
  • CRT (+15°C to +25°C)
  • Refrigerated (+2°C to +8°C)
  • Frozen (−25°C to −15°C)
  • Ultra-low (−85°C to −65°C)
  • In-house label design and production
  • Dedicated Returns area
  • Fully validated emergency backup generators
  • Annex 11/Part 11-compliant Inventory Control System,
  • Client portal (DashX), showing real-time progress of packaging, labeling, and shipment of supplies
  • Powered by solar energy and integrated backup systems

Facility Licenses & Certifications

  • MIA – Manufacturing / Importers Authorisation (Human Investigational Medicinal Products)
  • WDA – Wholesale Distribution Authorisation (Human medical products)
  • Certificate of GMP Compliance of a Manufacturer
  • Certificate of GDP Compliance of Wholesale Distributor