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Medical & Clinical Testing (often called clinical laboratory testing) involves analyzing patient samples (blood, urine, tissues, etc.) to diagnose diseases, monitor health conditions, guide treatment, and assess risk.
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Preclinical data is commercially useful only when it adheres to stringent global quality management frameworks
From stability testing and microbiological assessments to allergen and performance evaluations, these tests provide critical data for managing product quality and regulatory compliance.
With global supply chains expanding for repurposed anthelmintic APIs, robust third-party testing is essential to verify compound identity, ensure potency, and maintain strict regulatory compliance
By measuring the GI values of foods, laboratories provide essential information that guides dietary choices, supports diabetes management, and promotes overall health.
Understanding Urgent STAT Laboratory Tests: Key Diagnostic Tools for Critical Medical Care
Learn the phases, STAT vs. routine benchmarks, what affects TAT in contract testing, and how to specify TAT requirements when outsourcing lab work
How med-tech manufacturers are leveraging smarter material engineering and laboratory validation to hit sustainability targets without failing the FDA audit
Explore how lab service providers are using smart technology and digital evidence to adapt to stricter global regulations
Regulatory signals, audit expectations, and testing priorities labs should be preparing for as 2026 approaches
The path toward a clinically useful ovarian cancer early detection test lies in the development of sophisticated, multi-modal screening strategies.
CLIA inspections and evaluations assess a laboratory’s performance, record-keeping practices, and quality assurance protocols
Stay ahead with data-intensive, digitally connected, and regulation-driven clinical testing lab operations
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Connecting with accredited labs worldwide ensures your device moves smoothly through the FDA PMA review process
Investing in early phase potency assays and RMMs and aligning with GMP modernization can future-proof pharma testing labs
Labs are under pressure to deliver results that are not only accurate but also traceable, defensible, and structured for global compliance.
Expert sample management can bring in new therapies and devices into the market sooner and ensure they remain accessible and affordable
An in-depth analysis of the FDA's 2015 guidance for reprocessing reusable medical devices, driven by patient safety concerns in health care
A comprehensive overview of the 21st Century Cures Act for healthcare and research professionals, detailing its impact on innovation and patient care
Encapsulate success: Explore liposome research, characterization, stability, and safety testing for advanced drug delivery. Find expert labs for your needs.
Understand contamination risks, adopt proper technique, and maintain sample integrity across your workflows
Overcome common challenges in handling hydrogels and cell suspensions with reliable tools and standardized techniques
96-well ready-to-use kits enable precise profiling of disease-relevant deubiquitinating enzymes
Integrated DNA Technologies (IDT) has introduced the xGen Hybridization and Wash v3 Kit, a...
Innovative dry-format BAT enhances safety, speed, and scalability for research-use testing environments
Kill-step validation supports compliance, brand protection and market access, especially for companies exporting products or seeking SQF or BRCGS certification
Hydrogels have gained popularity due to their unique properties and applications in various fields, including medicine, agriculture, and personal care. This guide explores hydrogel testing, focusing on quality analysis, composition, testing methods, and regulatory requirements.
Influenza testing and research form a critical, interlocking system of patient care and public health preparedness.
Handheld contactless biomass sensor offers accurate cell density measurement in seconds
Ensuring standardization, accuracy, and efficiency in drug testing processes
Discover how each type of test serves distinct purposes, from immediate life-saving decisions to regular health monitoring, ensuring effective and timely patient care in various clinical scenarios
Understanding the operational parameters of HRP testing helps optimize and apply the assay better
The 2025 US outbreak, with 1,514 cases and three deaths, demonstrates what happens when vaccination coverage falls below the herd immunity threshold in a country that had sustained measles elimination for over two decades.
Technical analysis of static, dynamic, and fatigue testing methods are used to validate medical devices and implants, ensuring patient safety and predicting long-term in-vivo performance.
Technical guide to Hepatotoxicity (DILI) testing. Analyze liver injury mechanisms, advanced 3D models, Hy's Law, and regulatory compliance for drug safety assurance.
The biocompatibility standards get updated to encompass new materials and technologies, maintaining a high standard for patient safety and device efficacy
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