Drug Product
Analytical & Bioanalytical Services
Clinical Trial Supply & Logistics
Regulatory, Tech Transfer & Support Services
Company Overview
About
Tiofarma is a pharmaceutical CDMO offering comprehensive services.
Key Expertise
Specialized in Quality Control, Stability Testing, Method Development
Therapeutic Areas
Respiratory
Allergy
Quick Facts
HQ:Netherlands
Founded:2005
Employees:983
Capabilities & Services
Core Capabilities
- Biologics Drug Substance
- Biologics Manufacturing
- Formulation Development
Types of Organization
GMP Manufacturing
Quality Systems
Regulatory Support
Dosage Forms
Sterile Injectable
Containment Capabilities
OEB 4 (1-10 µg/m³)
Production Scales
Phase III Clinical Trials
Commercial Scale
Clinical
Markets Served
Global
Manufacturing Facilities
1 site worldwide
Tiofarma B.V.
Hermanus Boerhaavestraat 1, Oud Beijerland, 3261 ME
Site Capabilities
4 capabilitiesANALYSIS
LABEL
MANUFACTURE
PACK
International Regulatory
EU GMP Certificates
4
Regulatory Bodies
EMA/EudraGMDP
Regulatory Approvals
Drug Approval L7HPON
FDA · #APR-GWV1QX5G · 2022-05-01
Drug Approval H6ECM2
FDA · #APR-KSME9Q9I · 2018-02-01
Certifications
FDA Registration
U.S. Food and Drug Administration
Cert #: CERT-H2QE2CB8
Issued: 2020-10-21
Expires: 2025-08-23
ISO 13485:2016
International Organization for Standardization
Cert #: CERT-EXQZU1TW
Issued: 2020-02-22
Expires: 2025-04-14
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Key facts about Tiofarma
- Tiofarma is headquartered in the Netherlands.
- Tiofarma was founded in 2005.
- Tiofarma has 983 employees.
- Tiofarma has one manufacturing site listed on CDMO Hub, in Oud Beijerland, Netherlands.
- Tiofarma's capabilities include Biologics Drug Substance, Biologics Manufacturing and Formulation Development.
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