Pierre Fabre CDMO

Castres, France
Hybrid — also manufactures internal programs
Oral Solid Dose Finished Dosage Forms Non-sterile Liquids Semi-solids & Liquids Small Molecule API High-Potency APIs Packaging & Labeling
Program data pending ClinicalTrials.gov matching
Profiled
Not yet scored
○ FDA Inspections ○ Clinical Trials ○ SEC Filings ○ Press ○ EMA GMP ○ MHRA GMP ✓ HC GMP (4)

Quick Facts: Pierre Fabre CDMO

Signal Score
Profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed. How scoring works
Headquarters
Castres, France
Website
Modalities
Oral Solid Dose, Finished Dosage Forms, Non-sterile Liquids, Semi-solids & Liquids, Small Molecule API, High-Potency APIs, Packaging & Labeling
Active Programs
No ClinicalTrials.gov matches confirmed
Data Sources
FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring

About Pierre Fabre CDMO

Pierre Fabre CDMO makes its own pharmaceutical products and also offers contract development and manufacturing services. Capabilities: Oral Solid Dose, Finished Dosage Forms, Non-sterile Liquids, Semi-solids & Liquids, Small Molecule API, High-Potency APIs, Packaging & Labeling. 1 manufacturing site registered with the U.S. FDA and Health Canada. Website: https://www.pierre-fabre.com/en-us/innovation-and-partnerships/partnerships/contract-development-manufacturing

Signal Score

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

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 Pierre Fabre CDMO

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Not yet. Pierre Fabre CDMO is profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed.
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