Life Sciences
It’s a time of rapid change in the Life Science industry. Pharmaceutical and Biotechnology companies are facing a multitude of challenges: patent expirations, the need for higher quality
data in a faster timeframe, demand for compliance, and the overall accelerating cost of developing new drugs.
 In the fiercely competitive world of pharmaceuticals, the need for increasingly complex and powerful computing solutions has never been greater. Because when all is said and done, your
enterprise's ability to speed drug discovery, improve drug development processes, and bring drugs to market faster will largely depend on the technologies you use to store, analyze, and share
information to make those things possible.
Technology, if developed and implemented correctly, can significantly help a company increase their productivity thus reducing cost, accelerating time a drug comes to market, and optimizing
your overall drug development process.
What does d-Wise provide?
The d-Wise Life Sciences Practice builds custom solutions to solve Life Science industry problems and provides innovative technology to improve business processes. We deliver technology
solutions for customers by implementing and integrating existing technologies, building custom solutions, and developing business processes to optimize their technology. Our main goal
is to solve your problems and allow your organization to make better decisions during the drug development process.
How is d-Wise different?
The Life Sciences Practice brings a unique combination of 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 combined
with an understanding of 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.)
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