It’s a time of rapid change in the life science industry. Pharmaceutical and biotechnology companies face a multitude of challenges: patent expirations, the need for higher quality data in a faster timeframe, demand for compliance and the overall accelerating cost new drug development.
In the fiercely competitive world of pharmaceuticals, the need for increasingly complex and powerful computing solutions has never been greater. When all is said and done, your enterprise's ability to speed drug discovery, improve drug development processes and bring drugs to market faster largely depends on the technologies used to store, analyze and share information.
Technology, if developed and implemented correctly, can significantly increase a company's productivity by reducing costs, accelerating a new drug's time to market and optimizing your overall drug development processes.
What does d-Wise provide?
The d-Wise Life Sciences Practice builds custom solutions that solve industry problems by providing innovative technologies to improve business processes. d-Wise delivers technology solutions for customers by implementing and integrating existing technologies, building custom solutions and developing business processes to optimize technology. Solving your problems and allowing your organization to make better business decisions during the drug development process is d-Wise' main goal.
How is d-Wise different?
The Life Sciences Practice combines extensive domain knowledge in life sciences, a broad spectrum of technology expertise in a wide range of products and experience in implementing solutions in life sciences to provide a complete package for your company. d-Wise provides your company with agile, experienced software development professionals who understand the pains you face on a daily basis.
What experience does d-Wise offer?
- Experience in data warehousing, clinical programming, statistical analysis and FDA submissions
- Experience in CDISC, HL7 and other industry standards
- Planning and management of clinical trials
- Expertise in regulatory guidelines (GCP, 21 CFR Part 11, etc.)



Life Sciences
