Life Sciences companies are constantly searching for ways to better manage medical data and information in a secure and compliant fashion and be able to share information globally. SAS Drug Development provides a web-based repository for data, files, and documents that enables validation standards required by 21 CFR Part 11.
d-Wise provides expertise and experience in implementing SAS Drug Development in a compliant fashion. The Life Sciences Practice consists of former SAS employees who worked on the development and implementation of the solution. Their breadth of knowledge ranges from the technical architecture to the change management challenges of implementing SAS Drug Development.
d-Wise offers a wide range of implementation services to help your organization fully utilize the investment in SAS Drug Development
- Expansive knowledge of SAS Drug Development functionality and an understanding of how to apply it
- In-depth knowledge of the SAS Drug Development API and experience writing customized extensions and integrations
- Extensive SAS Drug Development implementation experience including change management, system validation and user acceptance testing, training, and documentation
- Broad experience working with international companies on global implementation projects
