Codis vs LGM Pharma

Auto-generated comparison by BioBM Editorial AI. This page highlights available profile evidence side by side and avoids drawing conclusions from missing fields.

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Category	Codis	LGM Pharma
Listed site	cdmo	cdmo
Summary	Global CDMO specializing in commercial-scale spray drying, amorphous solid dispersions, microencapsulation, and continuous granulation with 400,000 sq ft of GMP manufacturing across US and UK facilities.	LGM Pharma offers full-service CDMO support from concept through commercialization, plus API sourcing. It provides analytical method development and stability testing for APIs and drug products, with regulatory strategy support for 505(b)(2) and ANDA filings.
Services	Formulation Development Process Development CMC Analytical Development Stability Testing & Storage Quality Control Testing CMC Regulatory Submission Support Oral Solid Dosage Manufacturing Secondary Packaging & Labeling	CMC Analytical Development Stability Testing & Storage CMC Regulatory Submission Support Quality Control Testing
Modalities	Small Molecule	Small Molecule
Indications	Data not yet provided.	Data not yet provided.
Locations	Headquarters, St. Louis, Missouri, USA Microencapsulation & Continuous Granulation, St. Louis, Missouri, USA Spray Drying & Commercial Manufacturing, Haverhill, England, UK Manufacturing Facility, Nottingham, England, UK Manufacturing Facility, Seymour, Indiana, USA	Data not yet provided.
Certifications	FDA · Identifier: 21 CFR 210/211, 110/111, 117 German Authorities · Identifier: Manufacturing site GMP approval (Pharmaceutical Products Act)	Data not yet provided.
Reviews	Review summary appears after site-level review signal gate opens.	Review summary appears after site-level review signal gate opens.