Manufacturing
More TomorrowsTM
Helping you fast-track healthier futures.
As a purpose-fueled drug delivery CDMO, we leverage our specialist injectable, inhalation and dermal expertise to accelerate your product’s journey and make tomorrow’s possibilities a reality.
Innovative CDMO solutions
From development to commercial manufacturing and beyond, amplify your product’s impact with our exceptional-by-design CDMO solutions.
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Our Bridgeton facility has over 155,000 sq. ft. of dedicated aseptic operations space, including state-of-the-art laboratories and formulation suites, alongside almost 11,000 sq. ft. of fill suites to ensure the highest levels of quality and patient safety.
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Our legacy of innovation
History of Kindeva
Since 1956, we have been developing technologies that meet the demands of today and deliver the possibilities of tomorrow.
2024
Developing low-GWP inhalers
Developing low-GWP inhalers and planning the opening of one of the first commercial-scale green propellant lines for filling inhalers using propellants with up to 99.9% lower GWP than current options.
2012
Invented the CFC-free nasal MDI
Invented the CFC-free nasal MDI, a more environmentally sound device for drug delivery capable of bypassing the blood-brain barrier.
2010
Developed the first commercially available dose counter
Developed the first commercially available dose counter, ensuring patients knew the number of inhaler actuations remaining so they could always be prepared.
2009
Created the TruJect™ platform
Created the TruJect™ platform and introduced the next generation of easy and reliable single-chamber autoinjectors, widely used to deliver a variety of medications.
2005
Solid microneedle array patch development
Solid microneedle array patch development, creating accurate, reliable intradermal delivery with the potential to eliminate cold-chain storage and enhance immunogenicity and efficacy.
2002
Invented the BinaJect® platform
Invented the BinaJect® platform, bringing an industry-leading dual-chamber autoinjector option to market with enhanced stability and bioavailability.
1995
Launched the CFC-free MDI
Launched the CFC-free MDI and set the standard for future care options developed to help safeguard the environment.
1989
Developed the breath-actuated inhaler
Developed the breath-actuated inhaler, a lifesaving option for individuals with hand-breath coordination problems that make traditional inhalers difficult to use.
1970
Launched the drug-in-adhesive patch
Launched the drug-in-adhesive patch, providing a noninvasive method for delivering a drug over an extended timeframe.
1970
Invented the ComboPen® platform
Invented the ComboPen® platform to deliver medical countermeasures, which fueled autoinjector innovations for anaphylaxis.
1959
Created the emergency use autoinjector
Created the emergency use autoinjector, laying the groundwork for the ongoing refinement of self-administered injectables currently used by millions of people worldwide.
1956
Invented the pressurized metered‑dose inhaler (pMDI)
Invented the pressurized metered‑dose inhaler (pMDI) and kick-started the evolution of inhaled therapies by developing an easy-to-use device for patients around the globe.
Let’s transform tomorrow together
Every patient deserves a brighter tomorrow. As your strategic partner, we are dedicated to building your lasting legacy and helping you fast-track healthier tomorrows. You dream it, we deliver it.
Latest at Kindeva
Tomorrow’s in the making at Kindeva. Explore our latest insights and expert resources to advance your drug delivery development and manufacturing.
The bridge to uncompromising fill finish precision
Sterile fill finish is a sequence of tightly connected control points, where performance at each stage directly influences quality, timelines and patient safety. Bridgeton is designed to deliver control at every step of the fill finish journey. Our 155,000 sq. ft. aseptic facility combines advanced automation, gloveless isolator technology and structured process design to reduce […]
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The bridge to the future of sterile injectables
Access a sterile fill finish solution designed to help your product progress from formulation through commercial scale with greater confidence and control. Having invested over $200M in our purpose-built, Annex 1-aligned facility in Bridgeton, MO, we bring together the infrastructure, expertise and control needed to accelerate your path to market. From early development through to […]
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Your bridge to commercial sterile manufacturing
Sterile fill finish has changed. Annex 1 compliance and data transparency are no longer future considerations; they are the baseline. At the same time, programs are expected to move faster, scale seamlessly and maintain absolute control from the first clinical batch through commercial supply. Siloed models cannot keep up with the pace and control required […]
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Manufacturing more sustainable tomorrows for pulmonary care
The shift to more sustainable inhalers is gaining pace. As pressure grows to reduce their environmental impact, low-Global Warming Potential (GWP) propellants are becoming an important part of the future of metered dose inhaler (MDI) development. In this infographic, we explore the trends shaping that transition, and share how Kindeva is helping partners prepare for […]
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Parenteral precision: Annex 1-ready sterile fill finish by design
Parenteral precision is a blog series exploring the controls, technologies and design decisions that shape modern parenteral manufacturing. Each article looks at one capability through a practical lens: what it is, how it works, who it supports and why it matters. This first blog focuses on Annex 1-ready sterile fill finish. As the European Union […]
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Beyond the bench: Aerosol analysis and the physics of MDI performance
Modern drug delivery is built on an architecture of precision and predictability to ensure patient safety. Behind every successful inhalation therapy lies a methodical application of analytical science that characterizes the behavior of complex aerosol systems. In this Beyond the bench blog, we examine how this analytical backbone supports the development of pressurized metered-dose inhalers […]
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Powering every breath you give: Our world-class Loughborough site
Pulmonary drug delivery is undergoing a period of rapid change. Developers must bring increasingly complex therapies to market while preparing inhalers for the transition to low-Global Warming Potential (GWP) propellant technologies. Success depends on having expertise across formulation, device integration and scalable manufacturing capabilities. Kindeva’s Loughborough, UK facility stands ready for this evolution. Our global […]
Learn MoreParenteral capabilities overview
Next-generation biologics and combination products require precision and close coordination between drug delivery technologies and manufacturing execution. Kindeva advances parenteral programs across development and commercial supply by bringing together device expertise, aseptic manufacturing and scalable operations. Why choose Kindeva for your parental program Large-scale sterile fill finish The Bridgeton site supports vial, cartridge and prefilled […]
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Navigating the green revolution: Why next-generation propellants are critical for pMDIs
The imperative to address climate change is reshaping industries worldwide, and pharmaceutical manufacturers are no exception. In respiratory medicine, the spotlight has fallen on pressurized metered-dose inhalers (pMDIs). While crucial for millions of patients, pMDIs harness propellants with a global warming potential (GWP) many times higher than CO2. This significant environmental footprint is a critical […]
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