Contract Manufacturing

Making a difference through contract manufacturing.

We have over 27 years of experience manufacturing high-quality, sterile medications for hospitals and medical facilities across America.

At a Glance

State-of-the-art laboratories on-site for every stage in the development process.
We produce and distribute more than one billion doses of respiratory medications and 503B products annually.
Our capabilities have grown with a $215 million investment and expansion.

Capabilities

Scale. Speed. Support. All under one roof.

From phase I product development support to small-scale lab batches to large-scale manufacturing, we can help you reach your production goals.

Lab Batch Production

We are continuously monitoring the market for drug shortages so we can quickly develop and scale-up the production of much-needed medications to support physicians and hospitals in the treatment of their patients.

Lab Batch Production

Lab Batch Manufacturing

Our at-scale capabilities allow us to move from lab batch production to large batch manufacturing of up to 1 million doses within 3-4 days –with minimal waste– helping to alleviate drug shortages rapidly.

Lab Batch Manufacturing

Scale Up

Our production facility can support the large-scale manufacture of solutions, suspensions, and emulsions (up to 9000 liters), as well as support the formulation process with in-house technology and equipment.

Scale Up

Stability Profiling

We have full-service laboratories for chemistry and microbiology with the infrastructure to manage, conduct, and store stability testing. We employ TLC integration and automation to monitor the conditions of our large-volume storage spaces and electronic inventory management to streamline the stability study process.

Stability Profiling

Test Method Development

Our Test Method Development group has the technology to perform bioequivalence studies and provide data through analytical method validation to help meet regulatory requirements for the manufacture of generic drugs.

Test Method Development

Formulation

Our laboratories can support Phases I, II, and III clinical trials with basic research and formula development for emulsification and solubilization properties that increase the bioavailability of your active pharmaceutical ingredients.

Formulation

Work with Nephron

For more than three decades, Nephron Pharmaceuticals Corporation has set the standard for quality, safety and innovation in pharmaceuticals manufacturing. Now, Nephron also operates an industry-leading 503B Outsourcing Facility division, which produces pre-filled sterile syringes, IV bags, IV bottles and luer-lock vials.

Let us show you how we can make an impact on your production goals with our unmatched speed, scale, and support.

Testimonials

“Nephron has been a bright spot during our struggles with drug shortages, and even fluid shortages, over the last several years. When we do have delays they are relatively short and communication about them is comprehensive and abundant. Nephron’s customer service can’t be beat, and they are often our first ask when we want to request a new compound.”

Jon Brown PharmD, MHA System Manager-Pharmacy Sourcing, Nephron 503B Customer

“I am grateful that Lou and Bill Kennedy see the University of South Carolina and our state as locations to further their commitment to pharmaceutical manufacturing with world class quality and efficiency.”

Dr. Harris Pastides Former President, University of South Carolina

“The Nephron culture values hard work and career advancement. Nephron is not just a place to work. It is a place to start, develop, and succeed in your career.”

Ashley Daugherty Chief Scientific Officer, Nephron