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As we are aware of Duplicate Drugs and its curse to Indian people in daily news. The medicines manufactured in India are not upto international mark. I have my own experience while training Quality Control department  analysts  of  several  companies  throughout the county. For injections as per USFDA a special guideline is mandatory to check its Endotoxisn content. Endotoxins limit is mentioned for each finished and raw product in IP, EP, USP, JP as guideline to monitor Endotoxin. It shouldn’t cross the limit. If it is excess it may cause Kidney failure, Allergy, Fever, Immunological problems, Blood Clott, Infection, Headache, Respiratory problems even death in spite of of curing disease. To save money QC people are purchasing reagents used for this test and keeping it for company’s approval and audit, not for regular monitoring and testing. These irregulations should be stopped immediately to save life of Indians. To learn more on Bacterial Endotoxins Test visit <a href=”www.deepweb.today.com” title=deepweb-deep into the web of things “>deepweb-Today</a> and <a href=”www.tuubol.com”title=”TuuBol.com-Your Say”> Tuubol.com-Your Say</a>

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