IoT – Speeding up FDA Approval in Pharmaceutical Manufacturing


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


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


Java, Oracle, HTML, CSS, JavaScript, CKEditor


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.

We are eager to help you on your digital transformation journey

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