CDMO Services

Trust Your Molecule to the Masters

The capabilities of an enterprise. The focus of an entrepreneur.

Work with a CDMO advanced enough to take you all the way from initial research to successful launch—and lean enough to stay flexible, fast, and responsive to your needs along the way.

That’s an elusive combination. Fortunately, you’ve just found it in LGM Pharma.

Clear every regulatory hurdle.

Other submissions teams work at arm’s length from the lab. Not ours. We embed our regulatory specialists within the R&D lifecycle from day one, ensuring that every decision made in your project’s earliest phases sets you up for streamlined FDA approval.

Formulate every dosage form.

From blockbuster OSD forms to precisely formulated suppositories, our PhDs and analytical chemists know it all—and they have the end-to-end technology and quality manufacturing systems to turn that knowledge into your next high-quality commercial product.

Hit every manufacturing milestone.

Our U.S.-based facilities, which offer over 100,000 square feet of flexible manufacturing capacity, are engineered to deliver safety and compliance on an accelerated timeline. Our DEA-licensed locations also welcome projects that involve Class II-V controlled substances.

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Formulation Development

Our history of FDA approvals and successful product launches tells a story of rigorous quality-by-design.

Explore our approach to formulation development
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Solid Dose Delivery Systems

No matter its complexity, we have the skills and technologies to manufacture your next oral therapeutic.

Explore our approach to solid dose manufacturing
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Liquids and Suspensions

Trust your liquid or suspension project to the team that ships 10M cough & cold products each year.

Explore our approach to suspension drug forms
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Semi-Solids

We have the specialized skills and equipment to deliver creams, ointments, chewables, and more.

Explore our approach to semi-solid drug forms
Cbox cdmo suppositories - lgm pharma

Suppositories

You don’t get to 35M doses a year without knowing precisely how to manufacture this niche drug form.

Explore our approach to suppository drug forms
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Commercial Scale-Up / Facilities & Equipment

We support our clients’ scale-up, distribution, and reshoring from 3 fully equipped, US cGMP facilities.

Explore our facilities and equipment
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Regulatory Management

From NDAs to 505(b)(2)s, our submissions team knows what regulators expect—and how to deliver it.

Explore our approach to regulatory management