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Medical Devices Articles & Analysis

1,325 news found

Infection Control Resources to Detect Klebsiella and Other Pathogens in Healthcare Environments

Infection Control Resources to Detect Klebsiella and Other Pathogens in Healthcare Environments

For example, patients whose care requires devices like ventilators or intravenous catheters, and patients who are taking long courses of certain antibiotics are most at risk. ...

ByCochrane & Associates, LLC


THY Precision - Plastic Injection Moulding for Medical Devices: A Basic Overview

THY Precision - Plastic Injection Moulding for Medical Devices: A Basic Overview

⚫︎Key Materials Used in Medical Device Plastic Injection MouldingThe medical injection moulding process involves heating medical-grade resins until they become moulten. ...

ByHong Yang Precision Industry Co., Ltd.


Biopharma PEG Achieves FDA DMF Approval for HZ-PEG-HZ

Biopharma PEG Achieves FDA DMF Approval for HZ-PEG-HZ

The HZ-PEG-HZ (1K) product is critical for applications including: l Controlled Drug Delivery Systems: Leveraging its pH-sensitive hydrazone bonds for targeted and controlled release of active pharmaceutical ingredients in specific physiological environments (e.g., tumor microenvironments, endosomes, lysosomes). l Bioconjugation and Crosslinking: Facilitating the creation of stable linkages in ...

ByBiopharma PEG Scientific Inc


I.R. Tubes Pvt Ltd Expands Specialty Chemicals Portfolio to Support India’s Growing Industrial and Pharmaceutical Sectors

I.R. Tubes Pvt Ltd Expands Specialty Chemicals Portfolio to Support India’s Growing Industrial and Pharmaceutical Sectors

Tubes Pvt Ltd, a leading supplier of specialty chemicals in India, today announced the expansion of its product line to better serve the rising demand in pharmaceutical, medical device, and industrial manufacturing sectors. The company’s latest initiatives are aligned with India’s "Make in India" vision, aiming to deliver advanced chemical solutions that meet ...

ByI. R. Tubes Pvt. Ltd.


MedSource Labs in the Spotlight: NBC Nightly News with Andrea Mitchell

MedSource Labs in the Spotlight: NBC Nightly News with Andrea Mitchell

As shown in the segment that aired on April 25 on NBC Nightly News, tariffs have significantly affected our mission to manufacture and deliver medical supplies for our customers. Throughout our two-decade history, we have consistently adapted our business to respond to market changes, including the Great Recession and the COVID-19 pandemic. ...

ByMedsource Labs


Huateng Pharma to Showcase Extensive PEG Derivatives and CDMO Capabilities at CPHI Japan 2025

Huateng Pharma to Showcase Extensive PEG Derivatives and CDMO Capabilities at CPHI Japan 2025

Key Product Highlights: · PEG Derivatives o A vast inventory of over 3000 high-quality PEG derivatives. o Monodispersed PEG linkers and multi-arm PEGs. o Scalable production from R&D to GMP commercial levels. o Applications spanning ADCs, PROTACs, LNP drug delivery, medical devices, and more. · Pharmaceutical Intermediates o Comprehensive ...

ByHunan Huateng Pharmaceutical Co. Ltd.


Proregulations' Comprehensive EU MAA Solutions

Proregulations' Comprehensive EU MAA Solutions

Our service areas range from chemicals, pharmaceuticals, medical devices, cosmetics, food & dietary supplements to agrochemicals & biocides. Our featured services include but are not limited to FDA Medical Device Registration, 510(k) Premarket Notification, Drug Master File Document, FDA ANDA, FDA NDA, IND Application, ...

ByProregulations


Early Glycan Screening: Key to High-Quality Biologics Development, Upcoming Webinar Hosted by Xtalks

Early Glycan Screening: Key to High-Quality Biologics Development, Upcoming Webinar Hosted by Xtalks

In this free webinar, learn about the importance of early glycan screening for ensuring biologic quality, and how automation reduces time-to-insight and improves workflow efficiency. The featured speakers will share real-world applications and results from glycan screening success. Attendees will learn how to integrate automated glycan profiling into cell line development (CLD) labs. Early ...

ByAdvanced Instruments


Navigating FDA 510(k) Approval with Proregulations' Services

Navigating FDA 510(k) Approval with Proregulations' Services

U.S. medical device regulations require manufacturers of most class II and a small number of class I devices to file a 510(k) unless they qualify for an exemption. 510(k) is a premarket technical document submitted by the manufacturer to the FDA before the medical device product enters the US market to prove that ...

ByProregulations


MedSource Labs Celebrates Black History Month

MedSource Labs Celebrates Black History Month

Last year, during Black History Month, our team at MedSource Labs took a closer look at the world of medical illustration and the ongoing efforts to address the lack of diversity in the field. We were inspired by the work of medical illustrators who are breaking barriers and ensuring that healthcare visuals represent the full spectrum of patients they serve. ...

ByMedsource Labs


Proregulations Streamlines the U.S. Cosmetic Registration Process

Proregulations Streamlines the U.S. Cosmetic Registration Process

Our service areas range from chemicals, pharmaceuticals, medical devices, cosmetics, food & dietary supplements to agrochemicals & biocides. Our featured services include but are not limited to FDA Medical Device Registration, 510(k) Premarket Notification, Drug Master File Document, FDA ANDA, FDA NDA, IND Application, ...

ByProregulations


Proregulations Launches Comprehensive ANDA Services   

Proregulations Launches Comprehensive ANDA Services  

Our service areas range from chemicals, pharmaceuticals, medical devices, cosmetics, food & dietary supplements to agrochemicals & biocides. Our featured services include but are not limited to FDA Medical Device Registration, 510(k) Premarket Notification, Drug Master File Document, FDA ANDA, FDA NDA, IND Application, ...

ByProregulations


CD Bioparticles Introduces Endotoxin Free Silver Nanoparticles for Advanced Biomedical Research

CD Bioparticles Introduces Endotoxin Free Silver Nanoparticles for Advanced Biomedical Research

Silver nanoparticles (AgNPs) are increasingly being used in various fields due to their unique physical and chemical properties, including optical, electrical and thermal properties, high electrical conductivity and biological properties. These applications span the medical, food, healthcare, consumer and industrial sectors, with AgNPs being used as antibacterial agents, coatings ...

ByCD Bioparticles


STEMart Announces Balloon Catheter Testing Services to Ensure Medical Device Safety and Regulatory Compliance

STEMart Announces Balloon Catheter Testing Services to Ensure Medical Device Safety and Regulatory Compliance

STEMart, a US-based provider of comprehensive services for all phases of medical device development, announces the expansion of its medical device testing capabilities and introduces Balloon Catheter Testing Services for the development of safe and effective medical devices. ...

BySTEMart


Empowering Asthma Care: Bedfont® Scientific Limited Provides Vital Support for FeNO Testing in Response to Updated NICE Asthma Guidelines

Empowering Asthma Care: Bedfont® Scientific Limited Provides Vital Support for FeNO Testing in Response to Updated NICE Asthma Guidelines

Bedfont® Scientific Ltd., world leaders in breath analysis with over 47 years of knowledge in designing and manufacturing medical breath analysis devices, welcomes the recent update to the National Institute for Health and Care Excellence (NICE) guidelines on asthma management. Bedfont® manufactures the NObreath® Fractional exhaled Nitric Oxide (FeNO) ...

ByBedfont Scientific Limited


Proregulations Launches U.S. Drug Master File Document Production and Filing Service

Proregulations Launches U.S. Drug Master File Document Production and Filing Service

To sum up, Proregulations can offer support in activities like FDA Medical Device Registration, 510(k) Premarket Notification, Drug Master File Document, FDA ANDA, FDA NDA, FDA Cosmetics Registration, New Dietary Ingredients Compliance, Toxic Substances Control Act Compliance, FDA Agent Services, Medical Device Distributor ...

ByProregulations


Innovations in Medical Devices and Materials Used

Innovations in Medical Devices and Materials Used

The medical device industry is undergoing a transformative period marked by groundbreaking innovations and advanced materials. ...

ByFluorostore


Accelerated Aging Testing Services for Medical Devices

Accelerated Aging Testing Services for Medical Devices

STEMart, a US-based provider of comprehensive services for all phases of medical device development, has announced the launch of its new Accelerated Aging Testing Services for medical device manufacturers to ensure the long-term reliability and safety of their products. ...

BySTEMart


CDC Report: Burkholderia multivorans Infections Linked to Hospital Ice Machines

CDC Report: Burkholderia multivorans Infections Linked to Hospital Ice Machines

A Centers for Disease Control and Prevention (CDC) report published on October 3, 2024, linked Burkholderia multivorans infections to ice machines in multiple healthcare facilities in the western United States. This post summarizes key findings, implications, and recommended practices for healthcare providers to ensure patient ...

ByLiquitech, Inc.


Biopharma PEG Expands GMP Production of Lipids and PEGs to Meet Growing Demand for Lipid Nanoparticles

Biopharma PEG Expands GMP Production of Lipids and PEGs to Meet Growing Demand for Lipid Nanoparticles

By facilitating the development of cutting-edge therapies, our products support advancements in various medical fields, including gene therapy, vaccine creation, and oncology treatments. ...

ByBiopharma PEG Scientific Inc

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