The Bluesight Registry service is provided to Kit Check’s partners for the purposes of registering tags and items and is built based on policies and procedures that help pharmaceutical manufacturers and 503B compounders comply with their cGMP obligations.
Registry exposes various functions via API endpoints. They’re listed here and grouped by common production workflows.
API Endpoints & Use Cases
Tags & Items (Workflow 1) — In this workflow, the label converter registers tags first, then the manufacturer reads those tags during production of a specific batch and associates item data to them.
- Tags -> Create — Allows label converters to register new tags (EPC Layout v2, TID, etc.).
- Tags -> Add Item Data — Allows pharma manufacturers to add or associate item data (NDC, Lot Number, etc.) to previously-registered tags (EPC Layout v2).
Tags & Items (Workflow 2) — The manufacturer registers tag and item data for items in a specific production batch (the label converter hasn’t previously registered the tags).
- Tags -> Create and Associate — Allows pharma manufacturers to register item data (NDC, Lot Number, etc.) and related tags (EPC Layout v2) at the same time.
Drug Dictionary
- Drug Dictionary Overview — Allows pharma companies to manage their drug dictionary entries.
Additional use cases and API endpoints may be supported, but are currently beyond the scope of this documentation
Environments
In addition to the Production environment, partners can use our Integration environment for the purposes of software development and QA testing. Please work with your Kit Check representative to get the appropriate host names and environment-specific credentials.