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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Join us and become part of a CDMO dedicated to advancing our clients’ projects, ambitions and our industry.
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.
Built for better tomorrows: How Bridgeton delivers for patients
Kindeva’s Bridgeton facility offers a purpose-built solution for the complex and evolving landscape of injectable drugs. The facility was specifically designed to address challenges in sterile injectable manufacturing, such as the siloed approaches that often separate core functions like formulation and fill finish. By co-locating these functions and operating within integrated systems, the Bridgeton model […]
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Building confidence into complex drug-device programs with early analytical expertise
Drug-device programs are under pressure to do more, with tighter timelines, deeper scrutiny and increasing complexity. As teams move from concept through clinical and commercial phases, one challenge remains constant: ensuring products behave as intended, consistently and safely. That challenge gets more complicated as formulation, device mechanics, packaging and regulatory expectations converge. Whether developing an […]
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What makes Bridgeton the perfect partner for your next sterile fill finish project?
The pharmaceutical sector is experiencing a significant increase in the demand for advanced biologics, biosimilar therapies and other sterile injectables. As a result, the global sterile injectables market is projected to grow from $632 billion in 2025 to $1.078 trillion by 2032, with a compound annual growth rate of 7.9% [1]. In response to this […]
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From vial to value: How GLP-1s are redefining injectable care for chronic conditions
The market for glucagon-like peptide-1 (GLP-1) therapies is growing rapidly, with a projected value of $186.6 billion by 2032. Originally developed for diabetes, these therapies are now widely used for obesity treatment, which has created a need for convenient and scalable delivery systems. This growth is reshaping the industry, creating new demands on manufacturing capacity […]
Learn MoreThe Kindeva Advantage: Setting the Gold Standard for Elemental Impurities Testing
In this blog, Jen Roark, Scientific Director of Injectables at Kindeva, explores the challenges of controlling elemental impurities in drug products. She breaks down the risks and regulatory guidelines outlined in USP <232> and ICH Q3D, then takes a deep dive into the findings of a recent PQRI interlaboratory study that highlights the complexities of […]
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A bridge to the future: Our world-class Bridgeton facility
Manufacturing sterile injectables today is more complex than ever. Navigating stringent aseptic requirements, evolving regulatory expectations and the need for significant specialized investment has made the path to market increasingly challenging. A fragmented approach across development, drug substance manufacturing and fill finish remains a common industry practice that can introduce critical vulnerabilities. With every handoff, […]
Learn MoreMastering USP 661.1 and 661.2: Kindeva Drug Delivery Simplifies Your Path to Compliance
Understanding the evolution of USP <661.1> and <661.2> In this blog, Jen Roark, Scientific Director of Injectables at Kindeva, breaks down the critical shift in pharmaceutical packaging standards ahead of the fast-approaching December 1, 2025, implementation deadline. She covers the history of USP <661.1> and <661.2>, the move to a risk-based framework, specific testing requirements […]
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The impact of inlet design on HFA-152a pMDI drug delivery
When assessing aerodynamic particle size distribution (APSD) using the Next Generation Impactor (NGI), throat model selection can significantly influence drug deposition outcomes. Accurate deposition data is essential for optimising pMDI design and ensuring consistent, effective drug delivery to patients. Recent research by our pulmonary/pMDI experts—Aaron Taylor, Chad Haraldson, and Stephen Stein at Kindeva—explores how United […]
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Evaluating extractables in low-GWP pMDI formulations
As the pharmaceutical industry advances toward low global warming potential (GWP) propellants like HFA152a and HFO1234ze(E), understanding material compatibility becomes critical, especially when it comes to leachables from common device components. In a recent evaluation, a group of pulmonary experts at Kindeva assessed the extractable levels associated with various polybutylene terephthalate (PBT) suppliers in pressurized […]
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