JYMed

Shenzhen, Guangdong, China
Hybrid — also manufactures internal programs
Peptides Sterile Injectables
Program data pending ClinicalTrials.gov matching
Profiled
Not yet scored
✓ FDA Inspections (1) ○ Clinical Trials ○ SEC Filings ○ Press ○ EMA GMP ○ MHRA GMP

Quick Facts: JYMed

Signal Score
Profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed. How scoring works
Headquarters
Shenzhen, Guangdong, China
Website
Modalities
Peptides, Sterile Injectables
Active Programs
No ClinicalTrials.gov matches confirmed
Data Sources
FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring

About JYMed

JYMed makes its own pharmaceutical products and also offers contract development and manufacturing services. Capabilities: Peptides, Sterile Injectables. 1 manufacturing site registered with the U.S. FDA. Website: https://jymedtech.com/services

Signal Score

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

JYMed FDA Inspection History

2025-03
NAI VAI OAI
Date Site Type Observations Classification
2025-03-14
Hubei JXBio Pharmaceutical Co., Ltd.
Xianning 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 JYMed

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