Where Medical Innovations Take Flight
Discover American Preclinical Services (APS)
Whether your company is a startup or an established industry leader, APS can offer a full range of medical device and pharmaceutical testing from our AAALAC and ISO17025-accredited, USDA-registered, and GLP-compliant facility located in Minneapolis, MN.
By utilizing our catalogue of services, you will be able to develop and conduct a full Preclinical Research Program and chart a path for your product from proof of concept to regulatory submission, all while using the industry’s most advanced capabilities. Trust APS with any size or type of project, and experience the place Where Medical Innovations Take Flight.
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Preparing a wound care device for regulatory review means submitting the results from your preclinical wound care study. Whether it’s a mesh implant for hernia repair or medicated dressing designed to speed up healing for diabetic patients, the wound care…
When it comes to designing a GLP safety study for a medical device or process, selecting the appropriate animal model is one of the most critical elements. The challenge is that no animal matches the human anatomy. Dogs, pigs and sheep are quadrupeds, whi…