Drug Product
Analytical & Bioanalytical Services
Regulatory, Tech Transfer & Support Services
Company Overview
About
Prasfarma is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in Solid Dose Manufacturing, Oral Liquids, Topicals
Therapeutic Areas
Immunology
Rheumatology
Quick Facts
HQ:Spain
Founded:2001
Employees:1,638
Capabilities & Services
Core Capabilities
- Peptide Synthesis
- Small Molecule API
- Formulation Development
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Inhalation
Containment Capabilities
BSL-2 (Biosafety Level 2)
Production Scales
Phase II
Clinical
Pilot Scale
Markets Served
Europe
International Regulatory
EU GMP Certificates
2
Regulatory Bodies
EMA/EudraGMDP
Regulatory Approvals
Drug Approval 6N2GCS
PMDA · #APR-MHJGY058 · 2021-03-01
Certifications
ISO 9001:2015
International Organization for Standardization
Cert #: CERT-8AJIEGR5
Issued: 2020-09-20
Expires: 2025-08-21
ISO 13485:2016
International Organization for Standardization
Cert #: CERT-UDXPAW31
Issued: 2020-12-13
Expires: 2025-07-03
Health Canada GMP
Health Canada
Cert #: CERT-VNS17WAY
Issued: 2020-03-17
Expires: 2025-12-21
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Key facts about Prasfarma
- Prasfarma is headquartered in Spain.
- Prasfarma was founded in 2001.
- Prasfarma has 1,638 employees.
- Prasfarma's capabilities include Peptide Synthesis, Small Molecule API and Formulation Development.
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