The drug development process encompasses the rigorous journey from initial discovery to market approval, involving research, preclinical testing, clinical trials, regulatory approval, and post-market surveillance. It integrates scientific innovation, regulatory compliance, and ethical considerations to bring safe and effective treatments to patients worldwide.
Clinical trials are vital stages in the development of new medical treatments, therapies, and pharmaceuticals. These trials rigorously test the safety and efficacy of interventions on human subjects. Conducted in multiple phases, clinical trials adhere to strict protocols and regulations to ensure the reliability and validity of results. They involve diverse populations and are designed to assess various factors, including dosage, side effects, and long-term impacts.
Clinical trial phases are the sequential stages of drug development that assess safety, efficacy, and dosage. Spanning Phase I to IV, they evaluate experimental treatments in humans, starting with small groups and expanding to larger populations. Each phase generates critical data to ensure therapies meet regulatory standards and patient needs.
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