About Us

LGM Pharma is an innovation-driven API company, involved in distribution of quality cGMP pharma ingredients to leading pharmaceutical companies.


Aggregated Mindshare and Experience

Aggregated Mindshare &
Experience


Aggregated Mindshare & ExperienceWhether it is an ANDA, NDA or a 505(b)2 project, LGM has already supported hundreds of similar projects and has aggregated the mindshare and experience that has been an invaluable resource to our clients.

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Cost Effective APIs & Large Development Quantities


Cost Effective APIs & Large Development Quantities Based on your specific requirements, we can provide cost effective APIs for initial research and larger development quantities towards product commercialization

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Fully Accredited & Approved Manufacturing Sites


Fully Accredited & Approved Manufacturing SitesAll of our cGMP APIs originate from fully approved manufacturing sites. LGM Pharma is able to provide technical packages, letters of access (LoA) to filed DMFs and complete assistance towards any regulatory filings.

Our Capabilities

We specialize in supplying our customers with a wide range of APIs supported by integrated technical capabilities and access to complete regulatory DMF documentation, suitable for various R&D stages through commercial formulation production.

Our products originate from our API manufacturing partner sites who are approved by the leading health authorities, such as the US-FDA, EDQM, TGA, UK-MHRA etc. Some of the APIs that we supply are manufactured via non-infringing processes which would be suitable for Paragraph IV challenges / early launches in regulated markets.

Through competent assistance by our sales department, complete technical & regulatory capabilities and fast delivery of high quality ingredients at competitive prices, LGM has become a preferred API supply source.

Summary
Our Capabilities
Article Name
Our Capabilities
Description
We specialize in supplying our customers with a wide range of APIs supported by integrated technical capabilities and access to complete regulatory DMF documentation, suitable for various R&D stages through commercial formulation production.
Author
Publisher Name
LGM Pharma
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