While patient safety is paramount in clinical research and drug development, quality data is its most important output. But data is not enough: DIA's global professional network works to transform clinical, regulatory, and patient data into actionable information through the appropriate integration, analysis, reporting, and sharing according to aligned data quality standards.
Learning
DIA Digital Learning Catalog
DIA Learning programs provide unique, realistic opportunities for professionals to learn best practices in their fields with Internet-based courseware, conveniently accessible anytime, anywhere.
Electronic Regulatory Submissions Community
Our focus is on regional requirements, electronic submission technologies, electronic document formats and data, expanding types of electronic submissions, and current and emerging standards impacting electronic submissions.