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SAS Drug Development
Help for SAS Drug Development is accessible within the product.
Other SAS Drug Development documentation is distributed directly to customers.
Drug Discovery and Development with SAS®

SAS provides a centralized, integrated solution for managing, analyzing, reporting and reviewing clinical research information. This solution enables life sciences organizations to make informed business decisions with confidence, to assess the safety and efficacy of research compounds more effectively, to collaborate across trials, phases and therapeutic areas successfully, and ultimately get better products to market faster.
Available Drug Discovery and Development Solutions from SAS
SAS Drug Development provides an analysis and reporting solution that enables global collaboration with complete compliance and control.

SAS OnDemand: Drug Development offers small and midsize businesses a centralized, controlled, Web-based solution for efficiently developing, executing and managing the transformation, analysis and submission of clinical research data.
How SAS Is Different
Only SAS provides a secure, collaborative framework that puts controlled power into the hands of researchers who need it. The result is greater productivity and efficiency in these areas:
• Integration. Efficiently integrate and manage data from a wide range of sources ?such as electronic data capture (EDC) systems, in-house clinical data management systems (CDMS), labs and contract research organizations (CROs) ?while leveraging investments in existing systems and resources.
• Analysis and reporting. Accurately assess and report on study data in a timely manner. Efficiently generate presentation-ready statistical summaries of clinical trials data and easily share results with researchers or reviewers on demand.
• Discovery. Use your growing research information repository to rapidly investigate critical drug safety issues, pursue new marketing claims and explore potential product-line extensions.
• Regulatory compliance. Document research content via integrated processes that provide versioning, audit trails and electronic signatures, as well as fully describing the relationships between all process inputs, transformations, analyses and results.

应用于药物开发的SAS
SAS在药物开发中是有帮助的。

其他SAS药物开发文档直接发给客户。

药物发现和开发使用SAS ®

SAS提供一个集中，管理集成的解决方案，并分析，报告和审查临床研究资料。该解决方案为生命科学组织做出明智的业务决策提供保证，以评估其安全和疗效从而研究更有效的药物产品，使整个审判阶段和治疗领域的成功合作，最终获得更好的产品并更快推向市场。
一．可用于药物发现和开发的SAS解决方案
1.药物的SAS发展提供了一个分析和报告解决方案，可完全遵守和控制的全球合作。
2.需求的SAS：药物开发提供了中小型企业发展的有效集中，控制，基于Web的解决方案，执行和管理的转变，分析和临床研究数据并且给予提交。
二．SAS是如何不同的
只有SAS提供一个安全，合作的框架，提出控制的研究人员到谁需要它的人手中的权力。其结果是在如下领域提高生产力和效率：
1.集成。
有效地整合和管理多种来源的数据？如电子数据采集（EDC）系统，内部临床数据管理系统（收派管理系统），实验室和合同研究组织（CRO）？而在现有的系统和资源利用投资条件下。
2.分析和报告。
准确且及时地评估和研究数据报告。高效的生成并介绍临床试验数据的统计汇总，并随时方便地与研究人员或有需要的人评论分享成果。
3.发现。
越来越多的研究需要使用您的信息库，迅速调查关键药物的安全性问题，寻求新的市场要求和发掘具潜力的产品线及其扩展。
4.法规遵从。
文件，通过集成过程的研究内容，提供版本控制，审计跟踪和电子签名，以及充分描述所有进程的投入，转换，分析其因果关系。