Our strong relationships with world-class manufacturers around the globe reduces supply chain risks and improves your access to high-quality APIs. No matter how niche or complex your active pharmaceutical ingredient, LGM Pharma can secure it, import it, and deliver it to your door. From concept through commercialization, LGM Pharma's full-service CDMO will get your product to market faster-no matter your dosage form.
Protect patient health and your bottom line with a full continuum of analytical method development and stability testing for APIs and drug products. A continuum of robust support services, including analytical testing and stability studies. Many paths lead from early R&D to FDA-approved cGMP manufacturing, but only one will get you there on your timeline and with the quality you expect.
Protect patient health and your bottom line with a full continuum of analytical method development and stability testing for APIs and drug products. A continuum of robust support services, including analytical testing and stability studies. Many paths lead from early R&D to FDA-approved cGMP manufacturing, but only one will get you there on your timeline and with the quality you expect.
Services
Today, LGM Pharma is a global leader in sourcing APIs and manufacturing quality drug products for hundreds of clients, across a wide breadth of dosage systems. All of that began a century ago, when two brothers founded what would become LGM Pharma's contract development and manufacturing (CDMO) offering.
We maintain a database of high-quality APIs for virtually every therapeutic classification. The truth is, finding alternative salt forms, negotiating for unusual quantities, or synthesizing custom molecules isn't a much of a challenge for our API sourcing team-not with an obsessively curated manufacturing network like ours.
Bring us your "maybes" and we'll bring you the quality, speed, and supply chain security you need. We start with a bespoke approach to meeting your overall objectives, then we work backwards to address your API sourcing needs in a sustainable and scalable way. For example, are you planning to launch in the US or globally?
Secure your supply chain, and let LGM Pharma take the complexity out of API sourcing. We do it all to reduce the cost and risk of getting high-value active pharmaceutical ingredient to your doorstep, from connecting you with the right strategic API manufacturer to managing logistics and regulatory requirements.
Your 505(b)(2) project has tremendous potential, but finding the right active pharmaceutical ingredient manufacturer is complicated. The landscape is crowded, and you face increasing competitive pressure to get to market first. LGM Pharma's dedicated API sourcing team has been working with clients for years on the 505(b)(2) regulatory pathway and is currently supporting 100+ such programs across a wide range of therapeutics and at every stage.
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