Why Nova-Tech?

Focus & Expertise

We’re experts at manufacturing sterile animal health pharmaceuticals. It’s what we do. It’s all we do.

Our unwavering, exclusive focus on animal health products means we’ve developed a broad range of unique insight and deep expertise that you can leverage to your benefit. It means we’ve designed our facilities and processes to customize our services for the unique needs of the animal health customers.

You don’t have to worry about your animal health product taking a back seat to human health products that may be in the queue. That’s why North America’s top animal health distributors choose Nova-Tech as their go-to source for large volume parenterals and contract manufacturing.

We bring convenience, expertise and unmatched quality to the successful growth of your branded product and the expansion of your footprint in the U.S. marketplace.


U.S. Manufacturer

Our manufacturing facilities are right here in the U.S., centrally located in Grand Island, Nebraska. As a U.S. manufacturer, we are committed to working with U.S.-based companies throughout our supply chain-from ingredients to equipment, from packaging to transportation.

Our preference for U.S. suppliers means we can have greater confidence that we’ll have what we need when we need it-and that means fewer production disruptions. As a result, we help you mitigate the risks of import concerns that can affect the budget and schedule for your project.

Our long-standing relationships with our domestic suppliers allow us to improve efficiency, control costs and ensure quality at every step. As an added benefit, our partnership with U.S. suppliers helps strengthen our nation’s economy.


Responsive & Customer Focused

Nova-Tech is right-sized to offer you a powerful combination of high-quality manufacturing and unmatched customer service. Our flat organizational structure means you work directly with Nova-Tech professionals who can answer your questions, collaborate with you, and simply make things happen. As a result, your project moves through our facility efficiently-and you’re kept apprised of its status at significant milestones.


Straightforward Quoting

Thanks to our decades of experience and our animal health focus, we know the right questions to ask before we prepare a quote for you. When you get our proposal, you can have confidence that the numbers are reliable and the expectations are clear.



Our U.S. manufacturing facility is designed to produce a wide range of formulations and a wide selection of package sizes and materials including glass and HDPE for large volume and small volume parenterals. Our equipment, processes and procedures have been specifically designed for optimal flexibility so we can accommodate a variety of customer projects from routine orders maximizing efficiency to small batch developmental activities with special requirements. The combination of our animal health expertise and nimble structure also enables us to configure and quickly respond to shifts and opportunities in the marketplace.


Excellent FDA History

Nova-Tech has a long history of compliance with FDA GMP (Good Manufacturing Practices) standards. Our understanding of and strict adherence to Good Manufacturing Practices aids in the safety and effectiveness of your products.


Quality Management

Our Quality Management System is thoroughly integrated in the manufacturing process. Quality is deeply embedded in our culture and is maintained by our highly trained and motivated staff who are dedicated to the success of our customers and the integrity of the products we manufacture for them.

At the launch of each project, we utilize a master validation plan to help navigate through the change assessment needed for system design, equipment qualification, process validation and continued monitoring throughout the life cycle of the product or process. Our quality management services include:

  • Full documentation throughout the process
  • Vendor qualification
  • Annual product review
  • Customized stability programs
  • Method development and validation
  • Product, technology and method site transfer
  • SPL submission of labeler code, establishment registration and drug listing
  • Technical support
  • Project management