Your partner for
complex drug delivery

Getting every detail right, as efficiently as possible, within a global quality management system —from finalizing product design and method validation, to designing the clinical plan, leading and supporting studies, and developing and registering applications with regulatory authorities. Our program management experts are here to guide every step of the development process.

Your needs come first, and we have facilities to manufacture at just the right scale for your project. Whether you need support for clinical trials, regulatory data packages, process validation, or all of the above, Kindeva is here for you. For every step of the project, Kindeva customers should expect the expertise and highest standards of quality and regulatory requirements.

Customers come to Kindeva because our track record shows that we get products to market and seamlessly support them after launch. Commercialization projects are built upon quality agreements, continued process performance, supply chain management, and steadfast compliance with ever-evolving regulatory standards. Our global, cross-functional quality and regulatory teams make sure that your product’s performance meets expectations in the patient’s hands. Whether you commercialize with Kindeva from the start, or are looking to transfer your technology into our facilities, whatever your need, Kindeva has you covered.