Kindeva Drug Delivery announced the expansion of its analytical services capabilities — launching a new global business unit offering integrated and stand-alone analytical support to the wider pharmaceutical, biopharmaceutical, and medical device sector. For more than half a century, Kindeva has developed significant knowledge, experience, and expertise working on inhaled, injectable, and transdermal drug delivery development programs and cGMP commercial supply. Additionally, Kindeva has built deep expertise and capability in cGMP analytical services supporting its product development and supply partners.
In addition to increasing Kindeva’s global analytical footprint, Kindeva’s recently opened 32,000-square-foot state-of-the-art laboratories in Woodbury, Minnesota, will serve as the central hub for its expanded suite of stand-alone analytical services.
Kindeva will offer extractables and leachables, elemental impurities, medical device, and container closure integrity testing. Kindeva’s new container closure integrity testing to USP <1207> will be led by newly appointed Manager of Container Closure Integrity (CCI) and Medical Device Testing, Michael Dominguez, who recently joined Kindeva from DDL Testing. Dominguez brings deep expertise spanning a wide range of performance and functional medical device testing standards in deterministic CCI methods, including high voltage leak detection, vacuum decay, laser headspace analysis, and residual seal force testing. Kindeva’s extractables and leachables testing, and elemental impurities testing to ensure products comply with the ICH Q3D Guideline for Elemental Impurities, are led by Dan Dohmeier. Dohmeier’s team brings more than 60 years of extractables and leachables method development, validation, testing, and compound identification experience to address customer testing needs.
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