Drug Product
Analytical & Bioanalytical Services
Regulatory, Tech Transfer & Support Services
Company Overview
About
Fareva is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in Formulation Development, Process Development, Scale-up
Therapeutic Areas
Oncology
Hematology
Quick Facts
HQ:Luxembourg
Founded:1997
Employees:1,090
Capabilities & Services
Core Capabilities
- Oral Solid Dose
- Solid Dose Manufacturing
- Formulation Development
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Lyophilized (Freeze-Dried)
Sterile Injectable
Containment Capabilities
BSL-2 (Biosafety Level 2)
Production Scales
Phase II
Clinical
Pilot Scale
Markets Served
Europe
Manufacturing Facilities
1 site worldwide
FAREVA Mirabel
Route de Marsat, Riom, 63200
Site Capabilities
4 capabilitiesANALYSIS
LABEL
MANUFACTURE
PACK
International Regulatory
EU GMP Certificates
2
Regulatory Bodies
EMA/EudraGMDP
Regulatory Approvals
Drug Approval V1A1EV
Health Canada · #APR-LJNU4COM · 2019-03-01
Case Studies
0 published case studies showcasing past projects, challenges and outcomes.
Certifications
FDA Registration
U.S. Food and Drug Administration
Cert #: CERT-A0V34IV3
Issued: 2020-08-22
Expires: 2025-08-23
EMA GMP Certificate
European Medicines Agency
Cert #: CERT-D8CB8W6M
Issued: 2020-01-25
Expires: 2025-12-14
MHRA GMP
UK Medicines and Healthcare products Regulatory Agency
Cert #: CERT-WFL3AS1V
Issued: 2020-04-27
Expires: 2025-05-07
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Key facts about Fareva
- Fareva is headquartered in Luxembourg.
- Fareva was founded in 1997.
- Fareva has 1,090 employees.
- Fareva has one manufacturing site listed on CDMO Hub, in Riom, France.
- Fareva's capabilities include Oral Solid Dose, Solid Dose Manufacturing and Formulation Development.
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