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11200 Hudson Road , Woodbury, MN, 55129, US
Kindeva Drug Delivery is a global contract development and manufacturing organization focused on drug-device combination products. We develop and manufacture products across a broad range of drug-delivery formats, including pulmonary and nasal, injectable, and transdermal. Our service offerings span early-stage feasibility through commercial scale drug product fill-finish, container closure system manufacturing, and drug-device product assembly. Kindeva serves a global client base from our state-of-the-art manufacturing, research, and development facilities located across the U.S. and U.K.
CEO discusses drug delivery trends, recent advancements, sustainability efforts, and capacity expansion.
Released By Kindeva Drug Delivery
This webinar will provide a detailed look inside Kindeva’s state-of-the-art aseptic fill-finish facility. Attendees will learn how Kindeva’s advanced capabilities, cutting-edge technology (including the OPTIMA sterile fill-finish system) and commitment to progression can streamline the development and manufacturing of injectable drug products. The successful completion of the first registration batches at Bridgeton will also be […]
Aversa Fentanyl holds the potential to become the world’s first abuse-deterrent opioid patch.
By: Charlie Sternberg
The treatment will be stockpiled and available for rapid deployment as part of the SNS CHEMPACK program.
Combining Emervax’s emxRNA with Kindeva’s microneedle patch technology aims to allow for ease of transport and administration of vaccines.
By: Kristin Brooks
Prakash brings more than 25 years of experience leading IT, data and digital functions leveraging emerging technologies to boost productivity.
Bridgeton, MO facility ready to provide injectable fill-finish capabilities.
Discover strategies to optimize the human factors engineering process for injectable products.
By: Amy Lukau
Commercial Head of Injectables and Health Security for Kindeva Drug Delivery talks about the Bridgeton, Missouri aseptic injectable fill-finish facility.
By: Tim Wright
The new analytical services site is now FDA registered and classified as Voluntary Action Indicated (VAI) with regards to cGMP.
Doubles Kindeva’s UK lab footprint, expands operations, and will relocate approximately 50 quality control employees.
New line will be capable of handling both HFA-152a and HFO-1234ze propellants.
Johnson will lead global operations for all Kindeva’s manufacturing, research, and development facilities located across the U.S. and U.K.
New Versynta microBatch underlines Kindeva’s injectable CDMO capabilities.
Samsung Biologics, Fujifilm Diosynth Biotechnologies, WuXi STA and more shared major news—including investments, expansions & acquisitions.
Riter brings leadership and expertise in analytical testing and will head up the new analytical services global business unit.
Whether it’s an imminent supply chain reckoning, or a raft of new modalities, excellent opportunities still abound for the “right” CDMOs.
By: Gil Roth
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