How do pharmaceutical laws regulate the testing of drugs?

In Florida, pharmaceutical laws regulate the testing of drugs through a three-step process. Step one begins with pre-clinical testing. Under this phase, a drug must undergo basic laboratory studies to determine the safety and effectiveness of the drug. During this phase, the drug is tested on non-human models such as animals, bacteria, and cell cultures. The results of this phase will be used to determine whether the drug should be tested further in humans. Step two is clinical testing. During this phase, the drug will be tested on human volunteers or patients for a period of time. During this phase, the safety and efficacy of the drug is further evaluated by researchers. This phase is closely monitored to ensure that any adverse effects of the drug are noted and reported to the appropriate authorities. Step three is post-marketing surveillance. After a drug is approved by the appropriate regulatory body, it must still be monitored for safety and efficacy. This involves looking at adverse events that may occur after a drug is on the market, as well as assessing long-term safety and effectiveness of the drug. These three steps are important components of how pharmaceutical laws regulate the testing of drugs in Florida. This process is designed to protect public health and ensure that only safe and effective drugs are available for use.

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How do pharmaceutical laws regulate the testing of drugs?

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