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.
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.
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.
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.
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.
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.
2002
Invented the BinaJect® platform
Invented the BinaJect® platform, bringing an industry-leading dual-chamber autoinjector option to market with enhanced stability and bioavailability.
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.
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.
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.
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.
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.
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.
Mastering USP and : Kindeva Drug Delivery Simplifies Your Path to Compliance
Understanding the evolution of USP <661.1> and <661.2> It’s hard to believe that United States Pharmacopeia (USP) General Chapters <661.1> Plastic Materials of Construction and <661.2> Plastic Packaging Systems for Pharmaceutical Use have been in existence for well over ten years now. These chapters were first published in Pharmacopeial Forum PF 39(5) for public comment […]
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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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The three key trends that will most impact drug development in 2025
The speed of change in the drug development and manufacturing sector requires its stakeholders to be proactive in understanding and addressing key trends and directions the industry is taking. As a global market of considerable size and significance, the value of which is anticipated to grow from $589.06 billion in 2024 to $632.71 billion in […]
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Microneedle array patch characterization recording
Microneedle array patches (MAPs) have the potential to transform delivery of medications and vaccines. While this innovative drug delivery format could result in improved efficiency across a wide range of therapeutics, it also brings critical challenges. To successfully move from concept to commercialization, MAP manufacturers must consider scalability, regulatory compliance, and other complexities. In this […]
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Microneedle array patch characterization presentation
Microneedle array patches (MAPs) are a transformative innovation in drug delivery, with the potential to redefine how medications and vaccines reach patients. MAPs promise a simpler, more effective way to deliver a wide range of therapeutics, but their journey from concept to commercialization is filled with critical challenges. From scaling manufacturing to ensuring regulatory compliance, […]
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Addressing top tech transfer challenges
Technology transfer represents a critical bridge between development and commercial manufacturing. This complex process — moving product and process knowledge between development and manufacturing teams or between different manufacturing sites — demands precision at every stage. The implications of technology transfer extend beyond knowledge sharing. Each decision during this process directly impacts manufacturing efficiency, regulatory […]
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Tech transfer commercial manufacturing mindset
Technology transfer (tech transfer) moves product and process knowledge between teams or partners and acts as a crucial bridge between ideation and commercialization. Especially for complex products like sterile injectables, a smooth tech transfer process is essential. In this white paper, discover valuable strategies to embrace a commercial manufacturing mindset from day one. Download your […]
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HFA152a green propellant capabilities
With evolving regulations and a growing push for sustainability, switching pressurized metered-dose inhalers (pMDIs) to green propellants is becoming increasingly essential. One of the most promising low global warming potential (GWP) options is HFA152a. In this white paper, we share insights on transitioning to HFA152a. Download your copy to discover: An overview of sustainability regulations […]
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