Aurore Life Sciences
Hyderabad, Telangana, India
Hybrid — also manufactures internal programs
Program data pending ClinicalTrials.gov matching
Profiled
Not yet scored
○ FDA Inspections
○ Clinical Trials
○ SEC Filings
○ Press
○ EMA GMP
○ MHRA GMP
Quick Facts: Aurore Life Sciences
- Signal Score
- Profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed. How scoring works
- Headquarters
- Hyderabad, Telangana, India
- Website
- https://aurorels.com/cdmo/
- Modalities
- Small Molecule API, Intermediates, High-Potency APIs, Controlled Substances
- Active Programs
- No ClinicalTrials.gov matches confirmed
- Data Sources
- FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
About Aurore Life Sciences
Aurore Life Sciences makes its own pharmaceutical products and also offers contract development and manufacturing services. Capabilities: Small Molecule API, Intermediates, High-Potency APIs, Controlled Substances. 1 manufacturing site registered with the U.S. FDA. Website: https://aurorels.com/cdmo/
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 Aurore Life Sciences
Does Aurore Life Sciences have a CDMO Signal Score?
Not yet. Aurore Life Sciences is profiled, not yet scored. Scores are published after regulatory evidence is attached and reviewed.
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