Drug Development Assistance

LGM Pharma is a preferred supplier to universities, drug discovery companies, biotech, many major pharmaceutical manufacturers and holds a current Central Contractor Registration for government contracts. By working in close collaboration with manufacturers worldwide, LGM has developed a reputation in the industry for being able to deliver rare and unique molecules for each stage of drug development.  Therefore, we can provide a wide range of novel R&D molecules throughout your drug development program, for any of the following stages:

 
Drug Discovery  

Drug Discovery

Supplying novel molecules for your "targets" of interest, LGM Pharma can provide lab scale quantities for your target evaluation research, pharmokinetics and lead optimization analysis.

LGM Pharma has several quality products in stock and ready to ship. Our logistics team is capable of shipping these products within 48 hours of your order!

See how LGM Pharma can assist you with your Drug Discovery stage needs... click here >

 
Pre Clinical  

Pre-Clinical Trials

We supply thousands of API’s worldwide from our extensive network of GMP manufacturing partners, many of which hold DMF’s.

Researchers rely on LGM Pharma for their critical projects by entrusting us to rapidly deliver molecules for pre-clinical and early-phase clinical projects, as well as clinical trial materials. And whatever the customer’s size, there is always the need for secure and on-time supply, something we consistently respond to. LGM effectively collaborates with its clients providing close customer support in order to successfully meet projects goals/timelines.

See how LGM Pharma can assist you with your Pre-Clinical Trial stage needs... click here >

 
Cllinical Icon  

Clinical Trials

At LGM Pharma our goal is to help move you quickly and efficiently from preclinical into clinical development. During the development process, LGM Pharma will adhere to your trial schedule, based on your needs. LGM Pharma supports clinical trial material manufacturing in support of Phase I-III stage development.

LGM Pharma has extensive knowledge and experience providing clients with suitable material to meet most countries regulatory agency requirements.

We can provide strong regulatory support and documentation for your regulatory filings. LGM Pharma’s materials are accompanied by the proper regulatory certifications.

See how LGM Pharma can assist you with your Clinical Trial stage needs... click here >

 
Commercial Icon  

Commercial Production

LGM Pharma can provide commercial scale quantities of APIs based on your regulatory requirements. We are committed to maintaining the highest standards of regulatory and environmental compliance.  Our manufactures hold the highest accreditations: US-FDA inspected & approved, WHO-GMP, COS, CEP, US/E/J-DMF and are designed to efficiently handle complex gram/kilogram to metric ton quantities for your finished dosage form manufacturing.

See how LGM Pharma can assist you with your Commercial finished dosage form production stage needs... click here >