QYResearch: The Global Tuberculin market is expected to reach 288 M USD by 2022
Tuberculin, also known as purified protein derivative is a combination of proteins that are used in the diagnosis of tuberculosis. This use is referred to as the tuberculin skin test and is recommended only for those at high risk. Injection is done into the skin. After 48 to 72 hours if there is more than a five to ten millimeter area of swelling the test is considered positive.
A tuberculin skin test (also called a Mantoux tuberculin test) is done to see if people have ever been exposed to tuberculosis (TB). The test is done by putting a small amount of TB protein (antigens) under the top layer of skin on the inner forearm.
Tuberculin, also known as purified protein derivative is a combination of proteins that are used in the diagnosis of tuberculosis. This use is referred to as the tuberculin skin test and is recommended only for those at high risk. Injection is done into the skin. After 48 to 72 hours if there is more than a five to ten millimeter area of swelling the test is considered positive. All tuberculins should comply with the WHO requirements for tuberculin.
According to QYResearch, The Tuberculin market is expected to grow at a CAGR of 5% from 219 M USD in 2016 to reach 288 M USD by 2022 in global market. The Tuberculin market is very concerted market; the revenue of top three manufacturers accounts about 63% of the total revenue in 2016. The high-end products mainly come from USA and Europe.
The leading manufactures mainly are Sanofi Pasteur, Zoetis, Par Sterile, SSI, Japan BCG, Thermo Fisher, Sanroad Biological, CNBG. Sanofi Pasteur is the largest manufacturer; its revenue of global market exceeds 27% in 2016. The next is Zoetis and Par Sterile.
There are mainly two types of Tuberculin market: PPD RT 23 and PPD-S. Tuberculin PPD RT 23 is used in the Mantoux skin test to diagnose whether a person is infected with Mycobacterium tuberculosis. Tuberculin PPD RT 23 is regarded a gold standard in the field and has been recommended by WHO since 1963. PPD-S (PPD-Standard) was provided as the reference product in the United States.
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