Accelerated Analytical Laboratories
Nathan Greenleaf has extensive experience in quality management and analytical chemistry, currently serving as the Quality Department Manager at Accelerated Analytical Laboratories since June 2021, where responsibilities include overseeing the Quality Management System and transitioning to an electronic format. Previously, Nathan held roles such as Quality Control Manager at ChemRite CoPac Inc., focusing on analytical testing methods for cosmetics and sanitizers, and as an Analytical Chemist at MPP Group, LLC, concentrating on HPLC and GC analysis. Nathan's background includes a strong foundation in quality control and technical support across various companies, including Hydrite and Alcami Corporation. Nathan holds a Bachelor's Degree in Chemistry from the University of Wisconsin-Milwaukee and an Associate's Degree in Chemical Technology from Milwaukee Area Technical College, along with a Bachelor of Applied Science in Secondary Education specializing in Chemistry and Mathematics.
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Accelerated Analytical Laboratories
Accelerated Analytical Laboratories is a full-service contract cGMP-testing laboratory. With a 19,000 sq ft laboratory facility and a staff passionate about FAST, RELIABLE, and ACCURATE results, we provide the testing services that industry-leading companies rely on again and again. On the cutting-edge of techniques and technology, we service the pharmaceutical, medical device, sterile compounding, cosmetic, and OTC (over-the-counter) manufacturer spaces with the comprehensive services and testing they continually RELY ON. Providing each client a dedicated project manager, our clients appreciate the transparency, focus on strict timelines, and attention to detail that we bring to each project. Accelerated Analytical Laboratories is passionate about QUALITY: ► Our state-of-the-art facility is ISO 17025 accredited, the highest standards for testing laboratories that ensure that an outcome is well documented. ► We practice the FDA's Current Good Manufacturing Practice cGMP regulations for pharmaceuticals that mandate CONSISTENCY and quality. With specialties in Microbiology and Chemistry, Compendia Methods (USP/ EP/ BP/ JP/ FCC), process and Method Validation, Facility Monitoring Services, Quality Control and Release Testing, as well as ICH Stability Storage, we deliver a DEPTH and BREADTH that is unique among testing laboratories. Almost every service and test is done in-house so that we can adhere to our unparalleled level of quality. FOLLOW US to receive useful content, timely updates, and insight into why we are the best at what we do. CONTACT US to schedule a conversation about how we can impact your quality and efficiency with our fast, reliable, and accurate services and testing.