Drug Product
Advanced Modalities
Regulatory, Tech Transfer & Support Services
Company Overview
About
Curida is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in API Manufacturing, Sterile Fill/Finish, Lyophilization
Therapeutic Areas
Rare Disease
Metabolic
Quick Facts
HQ:Norway
Founded:1990
Employees:2,221
Capabilities & Services
Core Capabilities
- Biologics Drug Substance
- Biologics Drug Product
- Biologics Manufacturing
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Prefilled Syringe
Sterile Injectable
Containment Capabilities
OEB 5 (≤1 µg/m³)
Cytotoxic / ADC Handling
Production Scales
R&D / Pre-clinical
Lab Scale
Pilot Scale
Markets Served
Asia-Pacific
International Regulatory
EU GMP Certificates
1
Regulatory Bodies
EMA/EudraGMDP
Regulatory Approvals
Drug Approval PY6040
Health Canada · #APR-Y1USSVN7 · 2020-03-01
Drug Approval I92CT5
EMA · #APR-D3WJQ2W4 · 2022-10-01
Case Studies
0 published case studies showcasing past projects, challenges and outcomes.
Certifications
FDA Registration
U.S. Food and Drug Administration
Cert #: CERT-BLRH4W2D
Issued: 2020-01-17
Expires: 2025-03-01
ISO 9001:2015
International Organization for Standardization
Cert #: CERT-ZCPF967O
Issued: 2020-08-10
Expires: 2025-03-14
MHRA GMP
UK Medicines and Healthcare products Regulatory Agency
Cert #: CERT-AQWLZICJ
Issued: 2020-02-23
Expires: 2025-08-06
Health Canada GMP
Health Canada
Cert #: CERT-Y8S7LLRZ
Issued: 2020-10-20
Expires: 2025-06-12
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Key facts about Curida
- Curida is headquartered in Norway.
- Curida was founded in 1990.
- Curida has 2,221 employees.
- Curida's capabilities include Biologics Drug Substance, Biologics Drug Product and Biologics Manufacturing.
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