Leading pharmaceutical companies are reinventing themselves. They’re adapting to tremendous pressure to launch blockbuster drugs more quickly, frequently, and cost-effectively, while minimizing risks of noncompliance. In doing so, they gather more clinical trials data, more often, at every stage of research and development.
But clinical trials data and compound data are often poor in quality. When this data is inaccurate and inconsistent across multiple systems, clinical trials fall behind schedule and go over budget, revenue opportunities are missed, and compliance with regulations is difficult without a great deal of manual effort. To address these challenges, companies involved in trials require robust technology to manage their clinical trials and compound data, and the transfer of data between Contract Research Orgnisations (CROs) and their pharmaceutical customers.
The Informatica solution for clinical trials data and compound data management lets you launch drugs more quickly, frequently, and cost-effectively, while minimizing noncompliance risk. It provides a trusted 360-degree view of clinical trials data, which includes the drug, compound, site, trial manager, researcher, university, investigator, hospital, and patient involved.
This solution is complemented by Informatica’s suit of data management products and solutions that ensure the curation and rapid transmission of high quality across all trials, systems, and research partners by:
Informatica data management technology is used by business and IT communities. These teams collaborate to improve efficiency, control costs. and ultimately enable their organizations to deliver quality medicines to patients more efficiently.