Manufacturing Capabilities

Our production complex is FDA-approved for the manufacturing and packaging of liquid and semi-solid products. At 33,000 square feet, our site includes an administrative building and a facility for Product Development, Quality and Operations. The production area includes several compounding rooms, as well as multiple filling and packaging lines, with capacity for liquids, creams, ointments, gels and suspensions, among other topical dosage forms.

Our skilled operators and compounders are trained in current Good Manufacturing Practices (cGMP). We rely on their technical and industrial expertise to operate state-of-the-art equipment, including our new high-speed tube filling and packaging line.

Peter and Tri

Facility Expansion


Our facility expansion is a game-changer. The most exciting part is that we are building our own future.

Peter Gallagher, Strategic Affairs

 

Click here to see the economic impact study for the expansion

We have started a significant expansion to our facility in order to meet increasing commercial demand, as well as install the capability to manufacture sterile injectable products. The first phase of this expansion began in early 2016 and includes the renovation of a new Product Development laboratory.

Operations Job Opportunities

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The second phase will be a sizable expansion to our topical manufacturing and packaging area, Quality labs and warehouse. We will also install an isolator-based production line for aseptically-filled and terminally-sterilized vial and ampule products.

As we grow, we are especially focused on finding talented candidates with technical and industrial backgrounds who can be trained to operate in this specialized manufacturing environment.

In addition to our own product portfolio, we also provide contract manufacturing services for topical pharmaceutical products to the order and specification of our customers.