Canyon Labs

With a wealth of knowledge in microbiology and molecular biology, Olivia Tateoka Brown has trained and managed dozens of scientists in both academic and industrial settings. Her expertise spans medical devices, in vitro diagnostic tools, pharmaceuticals nutraceuticals, and dietary supplements, from product testing to quality and compliance.    Olivia's dedication has been instrumental in securing ISO 17025 accreditation for Canyon Labs for several years. Olivia's deep understanding allow us to offer tailored solutions for our clients. Her advanced degrees and continuous education in microbiology, molecular biology, and biocompatibility underscore her commitment to her career and to her team at Canyon Labs. We are thrilled to have Olivia as part of our versatile team! Meet Olivia and discover what she's up to outside of the lab below!

Happy Independence Day! Today, we celebrate the freedom and opportunities that define our nation. It's a time to reflect on the values of courage, innovation, and unity that have shaped our country. Let's honor the spirit of independence by continuing to push boundaries and achieve great things. Wishing everyone a safe and joyous Fourth of July!

Any guesses on what's in the BIG box?! HINT: Wendy Mach is pretty darn excited about it!

Meet Sarah Rosenblum Ptach, the president of Canyon Labs. Not only is Sarah our leader and mentor, but she is also committed to the packaging industry and its advancements! Sarah has a vast knowledge of medical device and pharmaceutical services, as she co-leads initiatives for Kilmer Innovations in Packaging (KiiP) while also serving as a board member for the Medical Device Packaging Technical Committee (MDPTC) of the Institute of Packaging Professionals (IoPP). We are proud to have Sarah in her position as President of Canyon Labs, as an innovator and opportunist in the medical device industry. Get to know Sarah and her hobbies outside of the lab below! The Steadman Clinic | Michael Gallizzi MD,MS, FAAOS | Top Horse Trails

Get the full scoop on a NEW standard for safe testing practices! Visit https://lnkd.in/gvFBQPAY to learn about the evolution of ISO 17665:2024 and how it will impact processes for staff members and clients!

We're thrilled to highlight our Sr. Director of Technical Services, Wendy Mach. At Canyon Labs, Wendy provides SME support for packaging, microbiology, and sterilization services. She has been instrumental by leading the launch of many services, including our newest packaging lab. Wendy brings nearly 30 years of experience in medical device manufacturing and laboratory testing. She began her career in Minnesota, performing ethylene oxide (EO) and gamma radiation sterilization validations for seven years. During her time there, she also insourced microbiology tests for sterility assurance and managed equipment validations. Wendy is a recognized industry subject matter expert in ship testing, package strength, integrity, and microbial barrier tests. Her distinguished work in the industry led her to being selected to lead Dupont's 10-year Tyvek transition project. Join us in celebrating Wendy's impressive career and invaluable contributions to the field and the Canyon Labs team! 

Are you tired of batch-release bacterial endotoxin testing (BET) slowing down your manufacturing process? Our newest equipment addition to the microbiology lab can help. Check out the Charles River Laboratories Endosafe Nexgen-MCS!   The MCS allows us to significantly expand our throughput of endotoxin testing. Each machine can process 5 test articles simultaneously and allows for quantitative results within 20 minutes. We have invested in four MCS instruments able to run 60 samples per hour. Many manufacturers still rely on the traditional gel clot method, which can be time-consuming and costly. This device allows us to deliver consistent results in a timely and cost-effective fashion.    Let us help you get your devices to the field faster! Learn more about our range of services and in-house offerings at https://canyonlabs.com/

Our in-house Sterility Assurance testing capabilities include: Bioburden Testing: This test quantifies the level of viable microorganisms present on a medical device or pharmaceutical product.   Endotoxin Testing: Endotoxins are components of the cell wall of Gram-negative bacteria that can cause fever and other serious reactions in humans. Endotoxin testing ensures that medical devices and pharmaceuticals are free from harmful levels of endotoxins. Product Sterility: This involves verifying that a product or its components are sterile, meaning free from viable microorganisms. Biological Indicator (BI) Sterility: This test is used to monitor a sterilization process to ensure it remains effective after validation. The testing involves incubating the BIs and observing them for growth. Residual Gas Analysis: Certain sterilization methods, such as ethylene oxide (EO) sterilization, leave residual gases that can be harmful if not properly removed. Residual gas analysis ensures that these gases are within safe limits following sterilization. Trust Canyon Labs for reliable and accurate testing and consulting. Contact Canyon Labs to learn how we can be your reliable and accurate partner here: https://lnkd.in/gS6pHhm6

Need Help Navigating the Medical Device Maze? Check out our blog to learn about regulatory & quality considerations for bringing your next medical device to market: https://lnkd.in/gdVp-qnF

It has been exciting to connect with so many experts and innovators in the orthopedic field at the OMTEC Conference in Chicago, IL! Special thanks to our very own Wendy Mach for sharing her thoughts today on "Picking the Right Packaging System for Your Orthopedic Devices". Tomorrow, she is speaking again on "Five-Year Device Sterilization Plans". We are excited to have Wendy represent Canyon Labs.    Canyon Labs is your end-to-end consulting and testing partner for sterilization and packaging. Visit www.canyonlabs.com to connect with our team!