Uveous Pharma Manufacturing ERP is designed for designed for pharmaceutical
companies subject to cGMP guidelines as described in below cGMP FUNCTIONALITY
section 21 CFR Part 211.
Uveous Pharma Manufacturing ERP includes a quality status for each inventory record
as well as other features to satisfy current Good Manufacturing Practice (cGMP)
requirements. In addition to the functionality found in the standard version of
UVEOUS Pharma Manufacturing, the list below indicates some of the unique features
included in the Uveous ERP:
Inventory record includes release status, retest date, and expiration date.
Inventory records must be changed to release status prior to use in production
(i.e. material issue).
Batch Tracking Log includes batch record review dates, QC dates, corrections,
dispositions and other information associated with a batch record.
Retest/expiration dates are calculated automatically based on offset period
maintained in the Item Master. Batches with upcoming retest / expiration dates
are identified by generating the Retest / Expiration Date Report.
Vendor item records include vendor NDC number and audit rating for each vendor
part number. Customer item records include customer NDC number for each customer
Drug License registration number and expiration date for company, customer, and
vendor records. The setting for the DL registration requirement is set at the
item level and checked when adding customer orders and purchase orders.
Numerous inventory and batch record reports available to summarize batch record
activity and review batch status.