Trade Restrictions on Medical Equipment: Proceed With Caution — and Build Quality into Every Supplier Decision
When global supply chains seize up, the cracks in preparedness show up fast — not as abstract policy debates, but […]
Sterility Assurance
Validating Reusable Medical Devices: Sterility, Material Degradation, and Safe-Life Assessments in a Circular Healthcare Future
Healthcare and sustainability are converging in powerful new ways. Around the world, hospitals and manufacturers are rethinking their environmental impact
When Trade Policy Disrupts the Supply Chain: How Medical Device Testing Adapts Under Tariff Pressure
The medical device industry thrives on global collaboration. Components may be designed in Germany, molded in Malaysia, sterilized in the
The Hidden Risks of Medical Equipment Rentals: Why Validation and Sterility Assurance Matter More Than Ever
In an era where efficiency and flexibility dominate healthcare operations, hospitals across the United States are increasingly turning to medical
Why Medical Device Experts Are Challenging Traditional Chemical Testing — And How CMDC Labs Helps Bridge the Gap
Introduction Medical devices—from surgical instruments and implants to diagnostic equipment—touch millions of lives every day. Their safety and reliability are
Ophthalmic Devices and the Hidden Risks of Regulation & Safety
The global medical device industry is under constant regulatory pressure, but few categories face the unique challenges of ophthalmic devices.
FDA Warning: Unreliable Third-Party Data in Medical Devices
In September 2025, the U.S. Food and Drug Administration (FDA) issued a cautionary update to the medical device industry: unreliable
Sterility Challenges in Breathing Circuits: Lessons from the Hamilton Recall
In August 2025, Hamilton Medical recalled multiple breathing circuit sets after concerns emerged over their sterility assurance. For hospitals and
FDA Declares PFAS Polymers in Medical Devices “Safe and Currently Irreplaceable”: What That Means—and What It Doesn’t—for Medtech and Hospitals
When most people hear “PFAS,” they think headlines about “forever chemicals,” drinking-water advisories, and state bans on PFAS-containing consumer goods.
Hidden Risks in Reusable Medical Devices: Cleaning Challenges You Can’t See (Until It’s Too Late)
Hospitals and medtech manufacturers know the stakes: a single reprocessing failure can cascade from a quality glitch into a patient
Evolving Sterilization Standards: What Device Labs Must Validate Now
In March 2025, the FDA expanded its recognized consensus standards database to include updated sterilization guidance documents from AAMI (Association
13% at Risk: How Testing Labs Can Support U.S. Medtech Amid Tariff Headwinds
Recent trade developments have raised serious concerns for the U.S. medical device industry. With tariffs increasing sharply on imports from
Sterile Supply vs. Emissions: How Labs Must Adapt to EtO Relief
On July 17, 2025, the White House issued a proclamation that affects the entire medical device sterilization industry. It gave
Sterility Isn’t Optional: What the Latest FDA Recall of Surgical Mesh Teaches About Medical Device Testing
On July 5, 2025, the U.S. Food and Drug Administration (FDA) announced a Class II recall of Ethicon’s PROCEED Surgical
Best Practices for Bioburden Testing in Medical Devices: Ensuring Compliance and Patient Safety
Introduction In the world of medical devices, safety and compliance are of paramount importance. The potential risks of introducing harmful
Sterility Testing Protocols: Innovations and Trends in the Industry
Sterility testing is one shared crucial component of medical device industry and pharmaceutical biotechnology. Guaranteeing sterility in all such products
Sterility Assurance: Key Insights from CMDC Labs for Pharmaceutical Safety
When it comes to pharmaceutical safety, sterility assurance holds a central position. It ensures that products are free of microorganisms
Sterility Testing Innovations: CMDC Labs’ Approach to Modern Challenges
Sterility testing has long held a very crucial importance in the biotechnology and pharmaceutical industries. It is a process that
Sterility Testing in Biotechnology: Key Protocols and Their Importance
One of the single most crucial aspect of biotechnology is sterility testing specifically in developing and manufacture of pharmaceuticals, medical
The Evolution of Sterility Testing in Pharmaceuticals: From Traditional to Modern Methods
Sterility testing is among the most critical components of pharmaceutical quality assurance. It ensures that the products that are meant
Sterility Assurance: Understanding the USP Standard for Pharmaceutical Safety
Ensuring the sterility of pharmaceutical products is a cornerstone of patient safety and regulatory compliance. Sterility testing is a critical
Sterility Testing Protocols: Best Practices and Innovations from CMDC Labs
Ensuring the sterility of pharmaceutical products and medical devices is a critical component of quality control in the healthcare industry.
USP Revisions: Ensuring Pharmaceutical Sterility at CMDC Labs
Sterility testing is a cornerstone of pharmaceutical manufacturing, ensuring that products are free from viable microorganisms that could harm patients.
Advancements in Sterility Testing: CMDC Labs Leading the Way
Ensuring the sterility of medical devices, pharmaceuticals, and biotechnology products is critical for patient safety and regulatory compliance. Sterility testing
Sterility Testing Evolution: A Deep Dive into USP Revisions
Sterility testing is a cornerstone of quality assurance in the pharmaceutical and medical device industries. Ensuring that products are free
CMDC Labs’ Cutting-Edge Approaches to Sterility Testing
Sterility testing is a critical component in the manufacturing of medical devices and pharmaceuticals. It ensures that products are free
Sterility Testing: USP Revisions and Industry Impacts
Sterility testing is a cornerstone of pharmaceutical and medical device quality assurance. It ensures that products intended for sterile use
Elevating Sterility and Bioburden Testing: CMDC Labs’ Innovative Approach
Sterility and bioburden testing are critical components of quality control in various industries, including pharmaceuticals, medical devices, and healthcare products.
Upholding Pharmaceutical Sterility: A Deep Dive into USP Compliance
In the realm of pharmaceutical manufacturing, ensuring product sterility is paramount to patient safety and regulatory compliance. The United States
Elevating Sterility Testing Protocols: CMDC Labs’ Insights
In the intricate landscape of pharmaceuticals, the assurance of sterility stands as a cornerstone of safety and efficacy. At CMDC
USP Revisions: Impacts on Sterility Testing Protocols
Sterility testing is a critical aspect of pharmaceutical manufacturing, ensuring the safety and efficacy of drugs and medical devices. The
USP Revisions: Impacts on Sterility Testing Protocols
Sterility testing is a critical aspect of pharmaceutical manufacturing, ensuring the safety and efficacy of drugs and medical devices. The
Innovative Approaches to Sterility Testing at CMDC Labs
Sterility testing is a critical component of pharmaceutical manufacturing, ensuring the safety and efficacy of parenteral products. Traditional methods, such
Evolving Sterility Testing: From USP to Contemporary Practices
Sterility testing is a critical component of ensuring the safety and efficacy of pharmaceuticals, medical devices, and healthcare products. Over
Examining the Revisions of USP: Insights into Sterility Testing
In the realm of pharmaceutical and medical device manufacturing, ensuring product safety and efficacy is paramount. Central to this assurance
The Evolution of Sterility Testing: From USP to Advanced Methods
Sterility testing is a cornerstone of pharmaceutical and medical device manufacturing, ensuring the absence of viable microorganisms in products intended
Enhancing Sterility Testing Protocols: CMDC Labs’ Comprehensive Approach
Sterility testing is a critical component of pharmaceutical manufacturing processes to ensure the absence of viable microorganisms in drug products.
Achieving Sterility in Pharmaceutical Products: A Guide to USP Compliance
Sterility assurance is paramount in the pharmaceutical industry to ensure the safety and efficacy of medicinal products. The United States
Mastering USP: Sterility Testing Excellence
Sterility testing is a critical process in pharmaceutical manufacturing, ensuring that products are free from viable microorganisms. As per the
Revolutionizing Sterility Testing: CMDC Labs’ Innovations in Ensuring Product Safety
Sterility testing is a critical aspect of ensuring the safety and efficacy of pharmaceutical and medical device products. Traditional methods
Exploring Sterility Testing: Challenges and Innovative Solutions
Sterility testing stands as a cornerstone in ensuring the safety and efficacy of pharmaceutical products. However, this critical step in
Mastering Sterility Testing: Best Practices from CMDC Labs
Sterility testing is a critical component of quality control in the pharmaceutical and medical device industries, ensuring that products are
Ensuring Compliance: The Vital Role of AOAC in the Food Industry
In the dynamic landscape of the food industry, ensuring compliance with stringent safety standards is paramount. At the forefront of
A Comprehensive Examination of Sterility and Bioburden Testing Protocols
Sterility and bioburden testing are critical components of ensuring the safety and efficacy of medical devices, pharmaceutical products, and healthcare
Breaking Down USP: A Crucial Aspect of Sterility Testing
Sterility testing is a critical component of ensuring the safety and efficacy of pharmaceutical products. Among the various guidelines and
Behind Closed Doors: Understanding Sterility Testing in the Pharmaceutical Industry
In the intricate world of pharmaceuticals, ensuring the sterility of products is paramount to guaranteeing patient safety and maintaining the
