Laboratorium Ofichem

Netherlands
Small Molecule API Oral Solid Dose
Program data pending ClinicalTrials.gov matching
Profiled
Not yet scored
○ FDA Inspections ○ Clinical Trials ○ SEC Filings ○ Press ✓ EMA GMP (1) ○ MHRA GMP ✓ HC GMP (4)

Quick Facts: Laboratorium Ofichem

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

About Laboratorium Ofichem

Laboratorium Ofichem is a contract development and manufacturing organization (CDMO). Capabilities: Small Molecule API, Oral Solid Dose. 1 manufacturing site registered with the U.S. FDA and Health Canada. Website: https://ofichem.com/

Signal Score

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

Laboratorium Ofichem EMA GMP Compliance 1 certificates

2026-07
Compliant Non-Compliant
Certificate Site Country Inspection Date Status
NL/API 26/2062232B Laboratorium Ofichem B.V. Netherlands 2026-07-28 COMPLIANT
Source: EMA EudraGMDP · 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 Laboratorium Ofichem

Does Laboratorium Ofichem hold EMA or MHRA GMP certificates?
CDMO Signal tracks 1 EMA GMP certificate for Laboratorium Ofichem.
Does Laboratorium Ofichem have a CDMO Signal Score?
Not yet. Laboratorium Ofichem is profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed.
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