Automate your dispensary operation and integrate stock and production order information with your ERP
Paper-based pharmaceutical manufacturers spend more money than their electronic-based competitors on the cost of maintaining and storing records, as required by the FDA, (estimated $400 Billion Cost of Goods Sold (COGS*).
With Ci-DMS MES batch manufacturing records are maintained and stored electronically with version control and approval. Our customers benefit from electronic traceability enabling quicker audit preparation, and rapid response to audit questions.
Ci-DMS MES electronically manages the weighing and dispensing of manufacturing and packaging materials and the sampling of raw material lots.
It is used in healthcare environments worldwide to improve Good Manufacturing Practice (GMP).
It replaces paper-based processes, helping achieve better compliance while improving operational efficiency and productivity