Validating clinical trial data reporting

Posted by / 22-Oct-2019 14:01

This indispensable guide focuses on validating programs written to support the clinical trial process from after the data collection stage to generating reports and submitting data and output to the Food and Drug Administration (FDA).The authors provide practical examples, explanations for why different techniques are helpful, and tips for avoiding errors in your output.For further information, including about cookie settings, please read our Cookie Policy .

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Often, what can be found is very complicated and not directly applicable to SAS programming in the pharmaceutical industry.

Carol and Brian have consolidated a lot of information about clinical trial data report validation and presented it in a way that makes it accessible and usable by programmers at all levels.

This book provides a straightforward, concrete plan for meeting the complex validation requirements that clinical trial data reporting must adhere to.

By including actual sample validation checklists in the book's appendix, the authors have allowed readers to implement the suggestions in the book with just a little effort.""Having taught a pharmaceutical-focused SAS programming class since 1998 using two other SAS Press publications, I am thrilled to say that this book will be such a benefit to my class as well as to others in the industry.

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The authors have done a superb job of conveying their years of combined experience in the writing of this text.