DAZ Systems, Inc. has detailed experience supporting the product life cycle and regulatory requirements of Life Science companies with Oracle E-Business Suite.

As a Life Science company gains approval to sell their products in the United States or in the global market, it becomes essential to have a business system that can speed up time to market, adhere to detailed regulatory requirements and handle detailed product traceability through an often complicated supply chain. In addition there are usually required integrations to clinical data management systems, CAPA systems, adverse reporting systems, and other industry specific data. DAZ Systems, Inc. has experience implementing Oracle Business Suite for Medical Device and Pharma from startups to Fortune 500 companies and is well versed in xGMP requirements and the document deliverables required for validation.

Talk to DAZ about how we have implemented E-Business Suite for other Life Science companies.

  • Global Organization with Rapid Growth
  • Project Accounting and Collaboration
  • R&D Time Entry by Project, R&D Procurement
  • Process or Discrete Manufacturing ( with cGMP requirements)
  • Serial number and lot number traceability—backwards and forwards
  • Heavily scrutinized product labeling
  • Revenue Recognition / Deferred Revenue
  • Financial Management / Consolidation
  • Clinical Data Management
  • Adverse Event and Reporting
  • Corrective Action and Prevention
  • 21CFR Part 11 Compliance
  • System Validations