Overview
LGM Pharma provides comprehensive API sourcing, contract development and manufacturing (CDMO) services, and analytical testing for the pharmaceutical industry across the full drug product lifecycle. With cGMP facilities in California, Colorado, and Texas, they offer capabilities in liquids, suspensions, semi-solids, suppositories, endotoxin testing, rapid sterility testing, and stability services. Their investments enhance U.S.-based production and quality systems to meet regulatory standards.
Frequently asked questions
- What CDMO capabilities does LGM Pharma offer?
- LGM Pharma provides contract development and manufacturing for liquids, suspensions, semi-solids, and suppositories from cGMP facilities in California, Colorado, and Texas, supporting scale-up and reshoring.
- What analytical testing services are available?
- Services include analytical method development, validation, stability testing, endotoxin testing, rapid sterility testing, and chromatography/spectroscopy for drug substances, excipients, and products.
- What are LGM Pharma's geographic locations and regulatory compliance?
- Facilities are located in California, Colorado, and Texas, all operating under cGMP standards with a strong regulatory track record for API sourcing and drug product manufacturing.