PHARMACOKINETIC ANALYSIS RESOURCE CENTER

承包商应作为药代动力学资源，支持 该药的药代动力学(PK)和药效学(PD)方面 药物开发计划。 进行PK研究，以确定吸收和处置 在体内的药物和帕金森病研究，以确定 药物的药理作用。PK和PD研究提供了一种方法 确定剂量、血药浓度和药物浓度之间的关系 药理作用。PK和PD数据为 为进一步的临床开发选择有前景的药物和 用于合理设计给药方案。因此，PK和PD研究 对于开发有效的药物是必不可少的，而且 在药物开发的每个阶段都需要。主键和PD信息 这是食品和药物管理局(FDA)的一项要求。 用于批准新药。 承包商应编制协议，监督研究，以确保 符合FDA相关规定，编制和编辑数据，进行PK，PD 和统计分析，并准备报告。数据/报告将是 提交给FDA以支持INDS(研究新药)和 新药申请(NDAS)。

The Contractor shall serve as a pharmacokinetic resource in support of the pharmacokinetic (PK) and pharmacodynamic (PD) aspect of the medications development program. PK studies are carried out to determine the absorption and disposition of a drug in the body and PD studies are carried out to determine the pharmacological effects of a drug. PK and PD studies provide a means to determine the relationships among dose, plasma concentration and pharmacological effect. The PK and PD data provide a basis for the selection of promising medications for further clinical development and for the rational design of dosage regimens. Therefore, PK and PD studies are essential for the development of effective medications and are required in every phase of medication development. Pk and PD information of this sort is a requirement of the Food and Drug Administration (FDA) for the approval of new drugs. The Contractor shall prepare protocols, monitor studies to assure that pertinent FDA regulations are met, compile and edit data, conduct PK, PD and statistical analyses, and prepare reports. The data/report will be submitted to the FDA in support of INDs (Investigational New Drugs) and NDAs (New Drug Applications).