Life Sciences

Clinical trial studies for Investigative New Drugs (IND) are labor intensive; they generate copious amounts of paperwork for exchange between investigators, pharmaceutical sponsors, and regulatory agencies.

Ensemble can streamline the clinical trial process and reduce the time and cost of paper-based processes while ensuring data security.

We can help you:

• Reduce pre- and post-trial delays with standardized electronic processes.
• Eliminate the time and cost of paper-based processes, and streamline data submissions by integrating customized electronic documents into the clinical trial process.
• Enforce certification and verification of secure electronic documents from investigators by implementing SAFE (Signatures and Authentication for Everyone) digital signatures.
• Achieve immediate information sharing and problem solving in clinical trials by connecting investigators and sponsors in a real-time collaborative work environment.

Contact us to find out about other ways in which we can help you.

Ensemble is an Adobe Gold enterprise solution partner. We provide advanced requirements analysis, architecture, and implementation services involving Adobe LiveCycle®, Flex™, Acrobat®, and AIR™.