Discover how SCIEX solutions empower modern clinical laboratories with accurate and comprehensive LC-MS/MS workflows for in vitro diagnostic testing, transforming clinical data into meaningful and actionable results to improve patient care.
Discover how SCIEX solutions empower modern clinical laboratories with accurate and comprehensive LC-MS/MS workflows for in vitro diagnostic testing, transforming clinical data into meaningful and actionable results to improve patient care.
SCIEX is your partner in advancing healthcare through accurate and precise diagnostic testing. Expand your clinical laboratory testing capabilities with our comprehensive LC-MS/MS clinical diagnostics workflows and solutions. SCIEX robust and flexible portfolio of LC-MS/MS medical devices for in vitro diagnostic use empowers clinical laboratories so they can meet today’s diagnostic needs while future proofing tomorrow’s challenging assays with unparalleled performance.
Best-in-class performance and reliability for your most challenging clinical assays. Discover how the speed and versatility of the SCIEX MS/MS Citrine system can tackle your clinical lab’s toughest assays with unmatched robustness and sensitivity.
Webinar
Making sense of IVD-R for LC-MS
The In Vitro Diagnostic Regulation (IVDR) is the European Union’s new set of rules aimed at improving the quality, safety and reliability of IVDs. Watch this webinar to understand how the EU’s new regulation is impacting the in vitro diagnostic landscape in the clinical laboratory. Learn about the new requirements for lab-developed tests (LDTs) so that your laboratory is IVD-R compliant when it comes to developing LC-MS/MS-based in vitro diagnostics assays.
Blog
What the FDA’s final ruling on LDTs means for your clinical laboratory
On May 6, 2024, the FDA published a final rule seeking to regulate laboratory developed tests (LDTs) as medical devices under the Federal Food, Drug and Cosmetic Act (FD&C Act). Read this blog to understand how this final ruling is reshaping the landscape of LDTs in the United States and learn about the actions your clinical laboratory can take to prepare to comply with the new FDA requirements.
Unveil the benefits of mass spectrometry for your most challenging clinical assays with our portfolio of robust and sensitive LC-MS/MS solutions registered as Class I and Class A in vitro diagnostic medical device under FDA and IVD-R, respectively.
The 4500MD systems provide the required sensitivity and specificity levels for core clinical diagnostics applications. The versatility of these mass spectrometers enables clinicians to perform routine quantitative analysis for the ever-increasing everyday demands of the modern clinical laboratory.
The Citrine systems bring ultimate sensitivity and robustness to meet your most challenging clinical diagnostics assays. The Citrine systems provide speed and performance to increase your laboratory productivity today and address tomorrow’s clinical diagnostics and research needs.
Transform LC-MS/MS data into meaningful and actionable results to improve patient care with our suite of software solutions tailored to your clinical diagnostics applications.
Powerful LC-MS/MS control, streamlined data management and compliance for your SCIEX devices.
Seamlessly process and accurately quantify multiple analytes across numerous samples with flexible software.
Streamline your LC-MS/MS clinical diagnostic testing with a simple 4-step workflow and intuitive point-and-click interface.
Effortlessly process batch sample screening results with user-friendly and personalized reports.
Maintain your lab’s productivity and help to ensure continuous performance with dependable aftercare and support solutions, including system service plans, training, application support, and consultancy.
Hub
Clinical knowledge center
Access the clinical knowledge center to explore resources and education content to get the most out of your SCIEX clinical diagnostics IVD medical devices.
Solution guide
Return-on-investment (ROI) calculator
Explore this tool to help you assess the financial value of implementing mass spectrometry to your clinical diagnostic laboratory.
Document
LC-MS/MS planning and implementation guide
Expand the testing capabilities of your current clinical laboratory testing by incorporating LC-MS/MS.
Dan Holmes is a medical biochemist who leads a hospital-based laboratory medicine program that has been using tandem mass spectrometry for routine and esoteric clinical testing since 2008. His department’s clinical mass spectrometry focus is reflected in its research and teaching interests.
When a hospital patient with acute renal failure brings along a sample of the mushroom soup that poisoned him, how do you identify the specific toxin?