CZECH-GEN

Olomouc, Czech Republic
Hybrid — also manufactures internal programs
Small Molecule API
Program data pending ClinicalTrials.gov matching
Profiled
Not yet scored
✓ FDA Inspections (1) ○ Clinical Trials ○ SEC Filings ○ Press ○ EMA GMP ○ MHRA GMP

Quick Facts: CZECH-GEN

Signal Score
Profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed. How scoring works
Headquarters
Olomouc, Czech Republic
Website
Modalities
Small Molecule API
Active Programs
No ClinicalTrials.gov matches confirmed
Data Sources
FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring

About CZECH-GEN

CZECH-GEN makes its own pharmaceutical products and also offers contract development and manufacturing services. Capabilities: Small Molecule API. 1 manufacturing site registered with the U.S. FDA. Website: https://www.czech-gen.cz/en/

Signal Score

Profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed. How scoring works

CZECH-GEN FDA Inspection History

2024-09
NAI VAI OAI
Date Site Type Observations Classification
2024-09-26
Czech-Gen, a.s.
Olomouc Company-level
Drug Quality Assurance No Voluntary Action Indicated (VAI)
Source: FDA Data Dashboard · Retrieved Oct 31, 2026

Hiring Activity Beta

Built from public job postings when a company's own roles can be read. Job postings are signals, not statements by the company; each one below links to the original. How we collect this
No hiring data yet. We haven't found a public jobs feed for this company.
Source: public careers pages · Checked Oct 30, 2026

Frequently Asked Questions About CZECH-GEN

How many FDA inspections does CZECH-GEN have on record?
CDMO Signal tracks 1 FDA inspection for CZECH-GEN, sourced from the FDA inspection database. See the full inspection history above.
Has CZECH-GEN received an FDA warning letter?
CDMO Signal has no FDA warning letters on record for CZECH-GEN.
Does CZECH-GEN have a CDMO Signal Score?
Not yet. CZECH-GEN is profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed.
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