Computer software, databases, and expert systems for use in drug development, particularly relating to raw material sources, drug substance and equipment vendors, contract research organizations, manufacturing procedures including scale-up scale-up, quality control, pre-clinical studies, toxicology, pharmacology, pharmacokinetics, metabolism, pre-formulation, formulation development, stability, regulatory guidelines and approval process, Chemistry-Manufacturing-Controls (CMC), pre-approval inspection (PAI), New Drug Application (NDA), Investigational New Drug (IND) application, clinical trials, Absorption-Distribution -Metabolism-Excretion (ADME), and licensing

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