We wish our Nelson Labs interns well as they head back to school this week! We had an incredible batch of interns this summer. Each intern was assigned a scientific project in addition to work in the lab. They also engaged in weekly Lunch and Learn sessions to learn more about the different types of lab testing performed by Nelson Labs. Additionally, there were weekly social activities to provide opportunities for our interns and senior leaders to get to know each other while having fun. The internship experience was capped off with an intern fair, presentations to the Senior Leadership Team, and a barbecue. These interns were amazing! We hope they have a terrific school year, and we look forward to welcoming them back next summer. Interns: Kate Blaes, Hayden Bryant, Grace Degreef, Elin Stones, Brooklyn Larsen, Nick Dinger, Madeline Winters, Tyler Nelson
About us
Nelson Labs is a global leader in microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries. Nelson Labs serves over 3,500 customers across 15 facilities in the United States, Mexico, Asia, and Europe. We have a comprehensive array of over 800 laboratory tests supporting our customers from initial product development and sterilization validation, through regulatory approval and ongoing product testing for sterility, safety and quality assurance. We are regarded as a best-in-class partner with a strong track record of collaborating with customers to solve complex issues. Learn more about Nelson Labs at www.nelsonlabs.com. Safeguarding Global Health® - with every test we complete.
- Website
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http://www.nelsonlabs.com
External link for Nelson Labs
- Industry
- Biotechnology Research
- Company size
- 501-1,000 employees
- Headquarters
- Salt Lake City, UT
- Type
- Public Company
- Specialties
- Medical device sterilization, microbiology testing, analytical testing services, biocompatibility testing, package testing, sterilization validation, bioburden testing, bacterial endotoxin testing, reusable device studies, pharmaceutical testing, sterility testing, and extractables and leachables
Locations
Employees at Nelson Labs
Updates
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In a newly published whitepaper, Shiri Hechter and Aryo Nikopour address the critical role of container closure system (CCS) qualification in safeguarding parenteral and ophthalmic drug products. Titled “Qualification of Primary Container Closure Systems for Parenteral and Ophthalmic Drug Products,” the paper examines the regulatory landscape, testing methodologies, and risk-based approaches necessary to ensure CCS integrity. Drawing on Nelson Labs’ expertise in extractables, leachables, and integrity testing, the authors provide a practical roadmap to achieving compliance while protecting patient safety. Read the full whitepaper: https://ow.ly/HQKW50WJbxV #DrugDevelopment #PatientSafety #ContainerClosure #Ophthalmics #Parenterals #NelsonLabs
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📢Nelson Labs expands testing capabilities in Wiesbaden, Germany. To meet growing demand, we’re expanding our Wiesbaden facility with new laboratories focused on packaging validation and microbiological testing — strengthening our integrated sterility assurance offering. 🔬 Comprehensive services include: Integrity testing & strength testing Container closure integrity Microbial barrier testing Aging studies & distribution testing Enhanced bioburden, endotoxin, EtO residuals & BI sterility testing This expansion reinforces the synergy between Nelson Labs and Sterigenics, offering customers a seamless solution for testing and sterilization — all in one location. More information: https://ow.ly/jFTw50WLUo4 #PatientSafety #LabTesting
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Join our upcoming live webinar on Tuesday, August 26, 2025, at 1:00 pm ET: A Dive into Disinfection Validations of Non-critical Devices This session will explore critical considerations for disinfection validations, including selecting the appropriate level of disinfection, evaluating disinfection methods, and addressing common challenges during validation of non-critical devices. Nelson Labs Presenter: Breanna Barber By attending, you’ll learn how to select the right disinfection level for your device, explore common disinfection methods, and understand acceptance criteria and the challenges that come with meeting them. Don’t miss this opportunity to strengthen your understanding of disinfection validations and ensure your devices meet regulatory expectations. Register here: https://ow.ly/EbLL50WHOVC #MedicalDevices #Disinfection #Validation #NelsonLabs
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Nelson Labs is proud to celebrate 40 years of science and service this year. In our Science in Seconds series, we’re bringing you quick insights from our experts on the work that helps support our mission, Safeguarding Global Health®. This week, Chrystel Lloyd shares why strong collaboration between manufacturers, third-party labs, and hospitals is essential for successful device reprocessing. She explains how bridging the gap between design, instructions, and real-world use helps ensure patient safety and regulatory compliance. 📺 Watch now to see how Nelson Labs partners with customers to connect every link in the reprocessing chain. Learn how Nelson Labs can help support the reprocessing of medical devices: https://lnkd.in/gW7NByjU #ScienceInSeconds #Medicaldevice #Reprocessing
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Come join our team at the PDA Universe of Pre-Filled Syringes and Injection Devices Conference in Vienna, Austria! Mark your calendar for October 21-22, 2025. We invite you to visit us at booth 113. Our team will be delighted to assist you and provide any information you may need. For more information and to register: https://lnkd.in/gjmKDebC #PDASyringesConference #MedicalDevices #patientSafety #LabTesting
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A strong quality culture isn’t just a best practice—it’s an essential part of regulatory readiness and long-term success. One of our most recent webinars this year takes a closer look at how life science organizations can evaluate and elevate their internal culture using a new industry standard. Titled “Understanding PDA/ANSI Standard 06-2025: A Roadmap for Culture Change” this webinar explores the purpose, structure, and application of PDA/ANSI 06-2025, a landmark guidance designed to help organizations proactively assess and improve their quality culture. Presented by Susan Schniepp of Regulatory Compliance Associates (RCA) and Matt Cushing of Nelson Labs, the session dives into the practical tools and leadership behaviors that foster a culture of quality—backed by real-world examples, proven frameworks, and side-by-side comparisons to help you apply the standard within your own systems. Key takeaways include • Understand the core principles and structure of PDA/ANSI 06-2025. • Explore key enablers and leadership behaviors that foster a quality-first mindset. • Learn to identify cultural breakdowns and implement proactive improvements. • Discover real-life examples of quality culture challenges and how this standard can help. • Gain tools and frameworks to assess and evolve your organization’s culture with confidence. Whether you're responsible for quality systems, regulatory compliance, or organizational development this on-demand session provides a valuable roadmap for meaningful cultural transformation. Watch the full webinar here: https://ow.ly/CU6N50WCcJ1 #QualityCulture #LifeSciences #PDAANSI062025 #RegulatoryCompliance #LeadershipDevelopment #ContinuousImprovement #NelsonLabs #OnDemandWebinar
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One of our most popular webinars to date is now ready to watch! Titled “ISO 10993-1 Panel Discussion: Preparing for Updates in the New FDIS” this highly attended session brought together three of Nelson Labs' leading biocompatibility experts— Thor Rollins, Chris Parker, and Nicholas Christiano M.S., MBA—for a deep dive into the most impactful updates to the ISO 10993-1 standard in recent years. The panel breaks down key changes in the newly approved Final Draft International Standard (FDIS), including: • Enhanced risk-based approach • Clarified guidance and expansion on device classification • Increased genotoxicity application • Improved integration with ISO 14971 • Updated guidance on biocompatibility at end of life and for reusable devices • Updated or expanded guidance annexes and test methods With hundreds of live attendees and an active Q&A session, watching this on-demand webinar offers valuable insights for anyone involved in medical device safety, product development, or regulatory strategy. Catch the full on-demand webinar here: https://ow.ly/GSmm50WCcQX #Biocompatibility #ISO10993 #MedicalDevices #RegulatoryCompliance #QualityAssurance #NelsonLabs #OnDemandWebinar
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In a newly published blog, Phil Tuckett, Department Scientist at Nelson Labs, explores how a cutting-edge technology, MALDI-TOF mass spectrometry, is transforming microbial identification in the pharmaceutical and medical device industries. Titled “Advancing Microbial Identification: How MALDI-TOF Improves Speed and Efficiency,” the article compares this rapid, protein-based approach to the long-standing “gold standard” of genetic sequencing. While sequencing remains highly accurate, Tuckett highlights how MALDI-TOF dramatically reduces turnaround time from hours to minutes without compromising quality. By leveraging both technologies, Nelson Labs can provide faster, more efficient results while maintaining the high standards customers depend on. Coming Soon: MALDI-TOF microbial identification will be available at our Salt Lake City location starting August 25, 2025. Read the full blog to see how MALDI-TOF is streamlining microbial ID: https://ow.ly/a9c850WAaR1 #MicrobialIdentification #PharmaceuticalTesting #MedicalDevices #LabInnovation #QualityControl #SaltLakeCityLabs #NelsonLabs
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Our next seminar will be taking place soon in Chicago. This three-day seminar is designed to help MedTech professionals gain a strong foundation in essential testing to achieve efficient, accurate, and effective testing outcomes. Register before August 23 to receive a $150 discount. Registration deadline is September 5. Learn more and register here: https://ow.ly/G7Ht50WzBTi
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