Drug Product
Regulatory, Tech Transfer & Support Services
Company Overview
About
Xellia Pharmaceuticals is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in Quality Control, Stability Testing, Method Development
Therapeutic Areas
Infectious Disease
Quick Facts
HQ:Denmark
Founded:2000
Employees:2,394
Capabilities & Services
Core Capabilities
- Small Molecule API
- Small Molecule Drug Product
- Oral Solid Dose
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Oral Solid Dose
Containment Capabilities
BSL-2 (Biosafety Level 2)
Production Scales
Pilot Scale
Phase I Clinical Trials
Clinical
Markets Served
Europe
Manufacturing Facilities
3 sites worldwide
Xellia (Taizhou) Pharmaceuticals Co., Ltd.
108 Binhai Road, Jiaojiang District, Jiaojiang Dist., Taizhou, Zhejiang, 318000
Site Capabilities
2 capabilitiesANALYSIS
API MANUFACTURE
Xellia Pharmaceuticals ApS
Dalslandsgade 11, Copenhagen S, Region Hovedstaden, 2300
Site Capabilities
5 capabilitiesANALYSIS
API MANUFACTURE
LABEL
MANUFACTURE
PACK
Xellia Pharmaceuticals Ltd.
Szállás utca 1-3, Budapest, Budapest H-, 1107
Site Capabilities
2 capabilitiesANALYSIS
API MANUFACTURE
International Regulatory
EU GMP Certificates
44
Regulatory Bodies
EMA/EudraGMDP
Regulatory Approvals
Drug Approval 7CWU0B
EMA · #APR-FKH1WD63 · 2022-05-01
Case Studies
0 published case studies showcasing past projects, challenges and outcomes.
Certifications
EMA GMP Certificate
European Medicines Agency
Cert #: CERT-YQK7WBQ5
Issued: 2020-06-11
Expires: 2025-12-10
ISO 9001:2015
International Organization for Standardization
Cert #: CERT-XBERBGBR
Issued: 2020-12-28
Expires: 2025-12-23
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Key facts about Xellia Pharmaceuticals
- Xellia Pharmaceuticals is headquartered in Denmark.
- Xellia Pharmaceuticals was founded in 2000.
- Xellia Pharmaceuticals has 2,394 employees.
- Xellia Pharmaceuticals has 3 manufacturing sites listed on CDMO Hub, in Taizhou, China, Copenhagen S, Denmark and Budapest, Hungary.
- Xellia Pharmaceuticals's capabilities include Small Molecule API, Small Molecule Drug Product and Oral Solid Dose.
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