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The Medical Devices and Healthcare Products industry develops and manufactures a wide array of items, from simple disposables like gloves and syringes to complex implantable devices and diagnostic equipment, all with a primary focus on patient safety and efficacy.
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Learn how independent laboratory validation proves your processing equipment is safe, cleanable, and ready for the official 3-A Symbol
Integrating third-party laboratory testing into procurement process transforms unknown supply chain risks into defensible, data-backed certainty
How med-tech manufacturers are leveraging smarter material engineering and laboratory validation to hit sustainability targets without failing the FDA audit
An NRTL-certified product gets quicker market access, is known for consumer safety, and adds to the brand reputation
Explore how lab service providers are using smart technology and digital evidence to adapt to stricter global regulations
This specialized testing helps researchers predict product longevity, performance, and potential failure points
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Connecting with accredited labs worldwide ensures your device moves smoothly through the FDA PMA review process
Labs are under pressure to deliver results that are not only accurate but also traceable, defensible, and structured for global compliance.
Is your lab prepared for the next wave of regulatory, technological, and client-driven changes?
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 irritation testing for medical devices, from its scientific basis and a tiered testing approach to the regulatory landscape
A comprehensive overview of the 21st Century Cures Act for healthcare and research professionals, detailing its impact on innovation and patient care
Learn how Cytiva’s membranes, filtration systems, and sampling tools help ensure consistent, compliant microbiology testing
Identifying and segregating medical waste and adhering to safety regulations help labs working with hazardous materials stay compliant
Meeting Diverse Sample Processing Needs
Expand your contract testing services with beacon discovery
Learn how to optimize inventory and lab resources to sustainably improve storage management
Integrated DNA Technologies (IDT) has introduced the xGen Hybridization and Wash v3 Kit, a...
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.
Handheld contactless biomass sensor offers accurate cell density measurement in seconds
Ensuring standardization, accuracy, and efficiency in drug testing processes
E&L testing is essential for patient safety, compliance, and to ensure product quality.
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
This extensive guide explores the principles, methods, and significance of endotoxin testing, which is vital for ensuring the safety and efficacy of pharmaceutical and medical products.
Learn more about the rigorous assessment processes defined by AAMI standards to ensure that medical devices meet the necessary safety, efficacy, and performance benchmarks
As the medical device industry continues to evolve and innovate, the importance of sterilization validation will remain a key factor in ensuring the safety and success of medical products.
By evaluating shoes based on criteria such as support, cushioning, fit, and breathability, APMA ensures that footwear products meet high standards of foot health.
Explore the core technologies driving modern CCIT and learn how to source the right cGMP laboratory for your packaging validation
Biocompatibility testing is essential for the safe and effective use of medical devices, ensuring they meet rigorous safety standards and regulatory requirements.
Ensure your medical devices are ready for the market with reliable cleaning and validation services
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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