Changzhou SynTheAll Pharmaceutical (WuXi STA)
Quick Facts: Changzhou SynTheAll Pharmaceutical (WuXi STA)
- Signal Score
- Profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed. How scoring works
- Headquarters
- China
- Website
- https://wuxiapptec.com/
- Modalities
- Small Molecule API, Peptides & Oligos
- Active Programs
- No ClinicalTrials.gov matches confirmed
- Data Sources
- FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
About Changzhou SynTheAll Pharmaceutical (WuXi STA)
Changzhou SynTheAll Pharmaceutical (WuXi STA) is a contract development and manufacturing organization (CDMO). Capabilities: Small Molecule API, Peptides & Oligos. 3 manufacturing sites registered with the U.S. FDA and Health Canada. Website: https://wuxiapptec.com/
Signal Score
Changzhou SynTheAll Pharmaceutical (WuXi STA) FDA Inspection History
| Date | Site | Type | Observations | Classification |
|---|---|---|---|---|
| 2025-04-25 |
Shanghai SynTheAll Pharmaceutical Co., Ltd.
Jinshan District, Shaanghai
Company-level
|
Drug Quality Assurance | No | Voluntary Action Indicated (VAI) |
| 2025-03-07 |
Changzhou SynTheAll Pharmaceutical Co., Ltd
Changzhou
Company-level
|
Drug Quality Assurance | No | No Action Indicated (NAI) |
Japan-accredited overseas site (PMDA)
general (non-sterile) · 3 sites
- Shanghai, China · Shanghai SynTheAll Pharmaceutical Co., Ltd. — general (non-sterile) · valid to May 22, 2028
- Taixing, China · Taixing SynTheAll Pharmaceutical Co., Ltd. — general (non-sterile) · valid to Apr 30, 2030
- China · Changzhou SynTheAll Pharmaceutical Co., Ltd — general (non-sterile) · valid to Dec 17, 2029
PMDA accreditation of a foreign manufacturing site is recognition within Japan's regulatory system, not an inspection outcome. PMDA's list covers only manufacturing sites outside Japan, so a company's plants in Japan are not on it. Source: PMDA, list of accredited/registered foreign manufacturers (as of Oct 16, 2026), Public Data License 1.0 (terms)