Eurofins Biopharma Services (CDMO)
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Drug Product
Analytical & Bioanalytical Services
Clinical Trial Supply & Logistics
Regulatory, Tech Transfer & Support Services
Company Overview
About
Eurofins Biopharma Services (CDMO) is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in Quality Control, Stability Testing, Method Development
Therapeutic Areas
Neurology
Quick Facts
HQ:Luxembourg
Founded:2017
Employees:3,082
Capabilities & Services
Core Capabilities
- Cytotoxic / ADC Handling
- High-Potency API
- Sterile Fill/Finish
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Topical / Transdermal
Containment Capabilities
Cytotoxic / ADC Handling
Production Scales
Pilot Scale
Phase I Clinical Trials
Clinical
Markets Served
North America
Manufacturing Facilities
1 site worldwide
Eurofins BioPharma Product Testing Switzerland AG
Parkstrasse 10, Schoenenwerd, Solothurn, 5012
Site Capabilities
1 capabilityANALYSIS
Regulatory Approvals
Drug Approval V8Z1MU
FDA · #APR-JGOT3FRG · 2020-03-01
Case Studies
0 published case studies showcasing past projects, challenges and outcomes.
Certifications
EMA GMP Certificate
European Medicines Agency
Cert #: CERT-VXL9VAYP
Issued: 2020-10-17
Expires: 2025-03-07
ISO 13485:2016
International Organization for Standardization
Cert #: CERT-0ECASOXV
Issued: 2020-11-12
Expires: 2025-09-24
MHRA GMP
UK Medicines and Healthcare products Regulatory Agency
Cert #: CERT-HR1VQNIG
Issued: 2020-04-20
Expires: 2025-09-14
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Key facts about Eurofins Biopharma Services (CDMO)
- Eurofins Biopharma Services (CDMO) is headquartered in Luxembourg.
- Eurofins Biopharma Services (CDMO) was founded in 2017.
- Eurofins Biopharma Services (CDMO) has 3,082 employees.
- Eurofins Biopharma Services (CDMO) has one manufacturing site listed on CDMO Hub, in Schoenenwerd, Switzerland.
- Eurofins Biopharma Services (CDMO)'s capabilities include Cytotoxic / ADC Handling, High-Potency API and Sterile Fill/Finish.
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