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Highly Pathogenic Avian Influenza A(H5N1) Virus in Animals: Interim Recommendations for Prevention, Monitoring, and Public Health Investigations

Summary The purpose of this guidance is to outline CDC’s recommendations for preventing exposures to highly pathogenic avian influenza (HPAI) A(H5N1) viruses, infection prevention and control measures including the use of personal protective equipment, testing, antiviral treatment, patient investigations, monitoring of exposed

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Teprotumumab Treats Thyroid Eye Disease Across Age

NEW ORLEANS — Teprotumumab (Tepezza) works equally well in both older and younger patients with thyroid eye disease (TED) and regardless of TED duration, new data suggest.  TED is an autoimmune disease characterized by orbital inflammation and expansion of fat and muscles around the

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Hepatitis Kills 3500 People Each Day, Says WHO

The number of deaths from viral hepatitis worldwide increased from 1.1 million in 2019 to 1.3 million in 2022. These figures equate to approximately 3500 deaths per day due to the disease, which is the second leading cause of mortality from infectious

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Europe Strengthens Future Disease Defense

A network of health security agencies has been established in Europe and Central Asia to bolster the region’s preparedness to meet future disease threats. The Pan-European Network for Disease Control (NDC) was launched on April 22 by the World Health

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Drinking water

Key facts Overview Safe and readily available water is important for public health, whether it is used for drinking, domestic use, food production or recreational purposes. Improved water supply and sanitation, and better management of water resources, can boost countries’

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WHO releases HIV drug resistance report

WHO’s latest HIV Drug Resistance Report gives an in-depth picture of the extent to which drug resistance is growing, and the steps that countries are taking to ensure people will receive effective medicine to treat and prevent HIV. The report reveals that

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Good Clinical Practice (GCP) Requirements for Data Submitted from Clinical Investigations for In Vitro Diagnostic (IVD) Device Premarket Submissions

The FDA has established human subject protection regulations addressing requirements for informed consent and Institutional Review Board (IRB) review that apply to all clinical investigations of devices involving human subjects, including deidentified human specimens. Investigations of medical devices involving human specimens, including

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EU Takes Steps to Prevent Medical Device Shortages

In response to ongoing concerns about medical device shortages, the European Union (EU) Council has endorsed new measures aimed at addressing these challenges. The agreed-upon revisions not only focus on preventing shortages but also include updates to registration procedures for

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Picture of COVID-19 in Europe Is Complex

“COVID is here to stay,” emphasized World Health Organization (WHO) Regional Director for Europe, Hans Kluge, MD, at a press briefing on January 16, 2024. He stressed the need for continuing vigilance and efforts to keep the disease at the top of

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