LGM Pharma is a leading CDMO provider of comprehensive API sourcing and drug product contract development and manufacturing solutions to the pharmaceutical industry. We secure and optimize your supply chain with our extensive qualified API partner network, global drug product development and manufacturing facilities, and regulatory and market intelligence services delivering customized solutions that get your products to market faster. 
Full-service, expert support that accelerates the new product pathway. Now that’s smart.

• Established in 2005
• ISO 9001-2015 QMS certified company
• CGMP systems in accordance with ICH Q7
• Main business segments: R&D / Biotech / CDMO / Specialty Pharma Companies, New Drug Delivery Technologies (NDA/505b2) – with heavy concentration on injectables, transdermal, nasal, inhalation, ophthalmic & sublingual drug deliveries

Our products originate from our API manufacturing partner sites who are approved by the leading regulatory authorities, such as the US-FDA, EDQM, TGA, UK-MHRA, PMDA etc. 

LGM’s industry experience enables us to support our clients throughout the entire pathway of drug development, from discovery through commercial production. Based on the scale and scope of development projects with which we are involved, we are able to provide our customers with a seasoned perspective and valuable market insight.

LGM Pharma has enhanced its position as a leading supplier of newly approved APIs, including full technical documentation and regulatory support. 

Our Clients:
At LGM Pharma, our clients’ needs are our top priority, and we support our client base consisting of a diverse array of pharma companies, including:
• Contract Research, Development & Manufacturing Organizations
• Specialty Pharma and Novel Drug Delivery Systems
• R&D & Biotech Companies	
• Generic Pharma Companies
• Chemical Catalog Companies	
• OTC & Private Label Manufacturers
• Academic & Government Laboratories
• Pharmacy Compounding Industry

Pharmaceutical

LGM Pharma

LGM Pharma's headquarters in Boca Raton, FL, United States

The Irvine office likely focuses on project management, quality assurance, and regulatory compliance in scientific and engineering fields.

Irvine

The Rosenberg office focuses on quality assurance, compliance, and infrastructure support in the scientific and HR sectors.

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