At every stage of your product’s development and manufacture, Kindeva Drug Delivery accelerates results, reduces costs, and minimizes risks. Bring high-quality products to your patients around the world with comprehensive solutions scalable to your needs and guided by our deep knowledge of device and drug quality system requirements.
From development to commercial supply, we provide CDMO services including full product life cycle management as well as analytical, regulatory, and quality support.
Device & product development
75 inventions in use
Clinical supply
75 Years of combination product firsts
Commercial supply
~ 100 M Commercial Devices Shipped Annually
Pulmonary & nasal, injectable, and transdermal delivery technology supply
Aseptic fill-finish
Our state-of-the-art Bridgeton, MO, facility features unparalleled automation, Annex 1 compliance with every line. Our aseptic injectable fill-finish capabilities accommodate an initial capacity of 100M+ units per year. Across vials, cartridges, and syringes, combining forces with Kindeva ensures you meet surging injectable demand. By integrating sterile fill, device manufacture, and final assembly in one geographic location, we also save you time and money while reducing your carbon footprint.
Dive deeper into our full range of CDMO services, from discovery to commercialization.
Meet your goals at every stage
At Kindeva, your product benefits from unparalleled development and manufacturing solutions backed by hands-on know-how and scientific rigor. Regardless of where you are in your program, we help you gain forward momentum based on a legacy of delivering innovative products that yield exceptional outcomes.