Whether you are a contract manufacturer or produce your own pharmaceuticals, Deacom’s single-system ERP provides a simplified solution to your complex issues. We give you the ability to:
Validating an ERP system helps pharmaceutical manufacturers ensure that their processes are consistent and operate in accordance with industry standards. Deacom assists with the validation process, establishing documented evidence that, throughout its lifecycle, DEACOM ERP will consistently function in accordance with its pre-determined specifications and quality attributes. For pharmaceutical companies validation of the compliance outlined in FDA 21 CFR Part 11 is a critical aspect of the implementation of DEACOM ERP.
During the production process, DEACOM ERP provides the ability to see every lot that went into a production batch, as well as details for reports that include who received shipments, their full contact information, lists of all the materials used in a batch, and who specifically performed the transactions. Batch tickets are automatically archived in the system to fulfill FDA requirements during an audit.
With the capabilities provided by the DEACOM AutoFinisher, pharmaceutical manufacturers can have serial numbers automatically generated with their specifications defined in the ERP system itself – not a 3rd party bolt-on. It allows you to adhere to the DSCSA rules for serialization of individual units, cases, and pallets by tying together the ERP system and the production equipment responsible.
Additional capabilities that support your pharmaceutical manufacturing needs include:
Have a question about Deacom’s ERP software? Call us at 1-877-4-DEACOM. Or better yet...