How-to Guide: Governing and Maintaining Standards for Collecting Clinical Data
Investing in data standards plays a huge role in improving the quality of clinical studies. But often, people don’t use the standards correctly, there are too many variations, or the standards keep changing, preventing you from running efficient trials.
In order to improve the study experience for all stakeholders, there needs to be an effective standards program in place. This free guide outlines how to:
- Involve the right stakeholders from the start
- Only collect what’s required to support study objectives
- Determine when and how updates to standards should occur
Learn how to develop a standards program that has your full team’s buy-in and improves the efficiency and quality of your clinical trials.
Veeva is a leading global provider of industry-specific, cloud-based software solutions for the life sciences industry. Our solutions enable pharmaceutical and other life sciences companies to realize the benefits of modern cloud-based architectures and mobile applications for their most critical business functions, without compromising industry-specific functionality or regulatory compliance. Find out more at www.veeva.com.