NAMSA Acquires American Preclinical Services, Becoming the Preeminent CRO Leader in Interventional and Surgical Preclinical Research Solutions. To learn more about this announcement, we invite you to access NAMSA's Press Release, here. 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.
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.
Services
American Preclinical Services research professionals are proficient, productive, and have the expertise to successfully design and execute your standard and custom studies. The APS management team offers extensive experience in veterinary science, medical device research, toxicology, pharmacology, histopathology, and FDA and ISO quality assurance policy.
APS is a full service, AAALAC and ISO17025 accredited, USDA registered and GLP-compliant Contract Research Organization (CRO). Located in Minneapolis, MN, we specialize in medical device and pharmaceutical testing. Whether your company is a startup or an established industry leader, our experienced scientific staff will meet your research needs and timelines.
APS has an independent quality assurance staff that maintains compliance to ISO 17025 and FDA Good Laboratory Practices requirements. Our QA team participates in all study designs and performs multiple audits during each study.
APS operates a comprehensive quality management system accredited to ISO 17025, which applies to our processes for identification of client needs, test selection, test validation, test documentation, and reporting of results.Biocompatibility tests are also included under our scope of accreditation.
APS operates a comprehensive quality management system accredited to ISO 17025, which applies to our processes for identification of client needs, test selection, test validation, test documentation, and reporting of results.Biocompatibility tests are also included under our scope of accreditation.
Does finding an appropriate preclinical contract research organization (CRO) feel like daunting task? You're looking for that perfect partner - a company with a team that understands you, your goals, and the obstacles you must overcome to reach them. Meet the outstanding team of APS and their Preclinical Research Program.
Are surgical, biocompatibility, toxicology, and pathology services available individually?. Yes, all APS services are offered la carte. Biocompatibility, ISR, analytical and pathology services can be quoted individually or as a complete preclinical program. FDA and European guidelines are very similar and are approaching harmonization.
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