United Kingdom (UK)

Comprehensive Clinical Supply Services

Since 2016, Xerimis UK has been providing comprehensive clinical supply services through our GDP/GMP facility located in Theale, United Kingdom. Cornerstone to our services here are Qualified Persons (QPs). Our QPs understand the unique requirements for importing your investigational medicine and releasing to clinical sites in the UK, while our expert teams in packaging, labeling and distribution ensure accurate preparation and delivery of your supplies per study protocol.

Contact

Xerimis Ltd.
Unit A2 Access 12
Station Road
Theale RG7 4PN
United Kingdom
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+44 (0)118 930 6197
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London Heathrow Airport (30 minutes)

Email

Info@xerimis.com

Directions

Google Maps

Xerimis UK Facility Highlights

Onsite QPs for batch release, Certification, and QP Declaration
Secondary packaging rooms
Process-flow floor plan and cGMP/GDP compliance
Cold-room packaging areas (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 areas
Dedicated Returns area
Fully validated emergency backup generator
Annex 11/Part 11-compliant Inventory Control System
DashX client portal, showing real-time progress of packaging, labeling, and shipment of supplies

Facility Licenses & Certifications

MIA – Manufacturer’s/Importer’s Licence (Human Use)
MIA(IMP) – Manufacturer’s Authorisation for Investigational Medicinal Products (Human Use), including importation of QP certified IMPs from a country on the approved country import list (QP oversight)
MS –Manufacturer’s “Specials” Licence (Human Use)
WDA(H) – Wholesale Dealer’s Licence
Certificate of GMP Compliance of a Manufacturer
Certificate of GDP Compliance of a Wholesale Distributor