Pharmaceutical Materials Management

Pharma Materials Management

Solution Summary

Manufacturers, Laboratories and other GxP pharmaceutical organizations require 21CFRPart11 compliant materials management.  Slingshot’s eStock Pharma application meets these requirements.  From receipt and labeling through put away, sampling and testing, batch processing operations, picking and shipping, all transactions are carefully tracked and audited.  Single or dual electronic signature control is required whenever the quantity or material status is changed.  
Beyond simple materials management, pharmaceutical capabilities include support for inbound and outbound checklists, lot-control including stability testing, certificate of analysis collection, genealogy, pedigree tracking (TI, TS, TH), shelf-life monitoring, material / location compatibility (for temperature-controlled locations), electronic batch records and sell unit serialization (DSCSA).  
Slingshot’s Validation Assist Package provides the tools your Quality department needs to rigorously validate the applications.  eStock Pharma is highly configurable without programming allowing you to turn off unneeded functions and simplify your validation process.  Once configured, documentation matching your configuration is provided by Slingshot including a Functional Requirements Specification, Traceability Matrix, Operational Qualification and Installation Qualification test scripts.  
Stop relying on spreadsheets to track your pharmaceutical materials.  Eliminate the vast amount of paperwork a manual system requires.   Enjoy the security. SOP compliance, auditability and control provided by Slingshot’s validated materials management system.

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Stock Pharma Datasheet (PDF)