When you trust in a contract development and manufacturing organization (CDMO), you’re really trusting in people. Chemists, who understand the precise APIs and excipients you need. PhD formulators, who know how to develop your bespoke process and scale it efficiently. Regulatory specialists, who position your project for streamlined approval from day one.
These are the people of LGM Pharma. Your partners.
Together, we offer close to a century of combined experience in both sourcing your API and bringing it to market. Many of our clients have stayed with us for decades and through several successful commercial launches, including projects in the 505(b)(2), ANDA, OTC, and compounding pharmacy markets.
We’ve built this track record by focusing on a culture of true partnership.
When you work with us, you are a valued and equal member of our extended team. It’s not up to you to give orders—instead, it’s up to us to ask good questions, find novel solutions, and offer timely advice. We are a communication-focused, quality-driven team, and we’ll be with you for every step of every project phase, from strategic sourcing through streamlined regulatory review for both APIs and drug products.
On behalf of clients seeking unique APIs and elevated supply chain security, we actively maintain strong partnerships with an extensive global network of cGMP and EU/US-FDA inspected manufacturers. Our frequent on-site visits allow us to personally assess their quality, compliance, and readiness, while our purchasing power gives us leverage to negotiate wisely on behalf of our clients.
To properly serve our clients’ unique needs, we reinvented the typical CDMO internal structure through the lens of Quality by Design (QbD). As a result, we are uniquely integrated; for example, our regulatory submissions team is embedded within our R&D team, ensuring that every decision we make on behalf of your project will help—not hinder—your FDA approval process.
Over 100,000 square feet of US-based manufacturing and warehouse facilities.
Nearly 100 years of combined experience
Unparalleled global network of prequalified cGMP API manufacturers
6,000+ APIs delivered to our clients’ door in the last three years
Locations in California, Colorado, Florida, Israel, Kentucky, and Texas
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.
LGM PHARMA
Call Toll-Free: 1-800-881-8210
Corporate Headquarters:
6400 Congress Avenue, Suite 1400
Boca Raton, FL 33487, USA
