LGM Pharma
Boca Raton, United States (US) · Health and Medical
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Last verified
May 2026
#cdmo
#api sourcing
#supply chain management
#drug manufacturing
#drug development
#regulatory submission
#505(b)(2)
Overview
LGM Pharma is a leading CDMO provider specializing in API sourcing and drug product contract development and manufacturing solutions, based in Boca Raton, Florida.
We support a diverse range of pharmaceutical companies, including Contract Research, Development & Manufacturing Organizations, Specialty Pharma and Novel Drug Delivery Systems, R&D & Biotech Companies, Generic Pharma Companies, and more. Our core service is to accelerate the new product pathway from early development through commercialization, offering full-service, expert support.
LGM Pharma’s industry experience and global network of qualified API partners and manufacturing facilities enable us to deliver customized solutions that get your products to market faster. We are ISO 9001-2015 QMS certified and operate under CGMP systems in accordance with ICH Q7, providing robust regulatory and market intelligence.
We support a diverse range of pharmaceutical companies, including Contract Research, Development & Manufacturing Organizations, Specialty Pharma and Novel Drug Delivery Systems, R&D & Biotech Companies, Generic Pharma Companies, and more. Our core service is to accelerate the new product pathway from early development through commercialization, offering full-service, expert support.
LGM Pharma’s industry experience and global network of qualified API partners and manufacturing facilities enable us to deliver customized solutions that get your products to market faster. We are ISO 9001-2015 QMS certified and operate under CGMP systems in accordance with ICH Q7, providing robust regulatory and market intelligence.
Contact Details
+11-800-881-8210
info@lgmpharma.com
Boca Raton, United States (US), 6400 Congress Ave
+5
Founded
2005
Company Type
Private Limited Company
Employees
100-150
Categories
Keywords
#cdmo
#api sourcing
#supply chain management
#drug manufacturing
#drug development
#regulatory submission
#505(b)(2)
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