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The general drug development process is laboratory research preclinical research, including animal testing and basic safety tests clinical research, also known as human trials review, in which the FDA decides whether to approve the new drug post-marketing safety monitoring Using the information gathered from this process, the FDA will decide whether a drug requires a boxed warning
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Clinical services, including medical consultations and prescribing decisions, are provided by independent, licensed healthcare providers who exercise their own professional judgment
Innovative and Patented Liposome-Based Drug Carriers
Available from: Wang Y, Song X, Zhuang L, Lang H, Yu L, Yan X, et al
