IoT – Speeding up FDA Approval in Pharmaceutical Manufacturing

Challenge

This major pharma company required a new method for submitting applications for FDA approval, which was very laborious, costly, time consuming and error prone.

Solution

TeraCode developed a document creation and management platform that streamlines document creation for clinical trials and studies required for FDA approval.

Technology

Java, Oracle, HTML, CSS, JavaScript, CKEditor

Outcome

The workflow is now a repeatable, standardized process that reduces inconsistencies in output, produces documents ready for external approval to agencies like the FDA, and cuts overall approval times.