Processes don’t make success happen. People do.
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.
Our partnership with you
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.