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The Biomedical Advanced Research and Development Authority (BARDA) is a U.S. Department of Health and Human Services (HHS) office responsible for the procurement and development of medical countermeasures, principally against bioterrorism, including chemical, biological, radiological and nuclear (CBRN) threats, as well as pandemic influenza and emerging diseases.
The Chemical Biological Incident Response Force (CBIRF) is a Marine Corps unit responsible for countering the effects of a chemical, biological, radiological, nuclear, or high-yield explosive (CBRNE) incident, support counter CBRN terrorism, and urban search and rescue when CBRN incident.
CBRN disposal technicians taking part in a training exercise. Chemical, biological, radiological, and nuclear defense (CBRN defense) or Nuclear, biological, and chemical protection (NBC protection) is a class of protective measures taken in situations where chemical, biological, radiological, or nuclear (including terrorism) hazards may be present.
The report focused on four specific vulnerabilities: assessment of "enterprise-wide threats", situational awareness and data integration, biodetection technologies, and lab safety and security. [30] [31] Products currently being produced or under development through military research include:
The Emergency Management (EM) career field is the United States Air Force's (USAF) primary organization responsible for implementing an installation-level EM program. . Emergency Managers, also known by the Air Force Specialty Code (AFSC) 3E9X1, are the Air Force's subject matter experts for all non-medical Chemical, Biological, Radiological and Nuclear passive defense and consequence management m
The Global Health Security Initiative (GHSI) is a collaborative effort among several nations and organizations focused on strengthening global health security. [1] [2] [3] Established in response to the 2001 terrorist attacks, its primary goal is to prepare for and address public health risks related biological, chemical, nuclear terrorism, or pandemics.
The companies claimed, among other things, that the health warnings violated their free speech rights by compelling the companies to endorse the U.S. government's anti-smoking message through ...
The MedWatch system collects reports of adverse reactions and quality problems of drugs and medical devices but also for other FDA-regulated products (such as dietary supplements, cosmetics, medical foods, and infant formulas). As of the summer of 2011, the program had received more than 40,000 adverse event reports. [1]