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Cuban Resolution to Lung Cancer

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[Type the company name] | Cuban Revolutionary Lung Cancer Vaccine |

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Introduction
Every year many people of different ages suffer and die worldwide from different types of cancers. An estimate made by the American Cancer society states that, in the US alone, in 2014 cancer killed 585,720 and lung cancer was responsible of 159,260 deaths (Deadliest Cancer Coalition, 2014). Lung cancer has become the leading killer cancer and finding better ways to treat it has become a priority for many researchers. American Cancer Society. Cancer Facts & Figures 2014.
Depending on the type of lung cancer and how far …show more content…

Cuba VS US The U.S. Food and Drug Administration (FDA) is an agency within the U.S. Department of Health and Human Services that is responsible for assuring the safety, efficiency, and quality of drugs and vaccines. In America a drug must first be evaluated by the Center for Drug Evaluation and Research (CDER), which is a division of the FDA, before it gets approved for sale. This means that the department must make sure that the medicine been evaluated works properly and that its health benefits are greater than its identified risks. A company or a sponsor that is introducing the new drug initially performs a laboratory and animal tests to determine the safety and the effectiveness of the drug in humans. Once this step is successfully completed, several tests are implemented in people to confirm that the drug is safe when used to treat a disease and whether it provides a real health benefit. Finally, results of the tests that prove the safety and the effectiveness of the treatment are sent to the CDER. After a group of experts at CDER reviews the submitted evidence and ensures that the medicine's health benefits surpass its known risks, the drug can then be sold around the US (Development & Approval Process (Drugs), 2014). Similar to U.S.’s system, Cuba’s medical and biotechnology products, even though all drug distribution channels are owned by the government, are subject to clinical tests before authorization and marketing both in Cuba and in

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