Advanced Radiation Therapy Device Manufacturer

Advanced Radiation Therapy Device Manufacturer

Implements & Validates Microsoft Dynamics AX 2009

Case Study

Major Medical Device Manufacturer Implements & Validates Microsoft Dynamics AX 2009

The priority goal was the consolidation and global deployment of the integrated ERP system and new enhanced functionality.

  • Consolidated Financial Reporting

  • Integrated Quality Management

  • eDHR / DMR Management

The system was deployed

  • 21 CFR Part 11 Electronic Records; Electronic Signatures

  • 21 CFR 820.30 Device Design Controls

  • 21 CFR 820.100 CAPA

  • Ensure Compliance And Business Continuity

  • Maintain Spares Inventory in Multiple Locations

  • System Validation & Verification

  • 21 CFR Part 11 Compliance

  • Management Of Multiple Warehouses And Perform Requirements Planning On Multiple, Nettable Warehouses

  • Eliminate The Disparity Between The Sales Order Installation And Planned Shipment Date

  • Streamline Rework Orders Process

  • New Enhanced Approved Supplier List

Purchase Toolkit and/or Automated Validation Software Tool

yes

no

onshore professional services

validationPro-multicolor

Methodology and approach

To achieve the objectives for this client, Fullscope assembled a team of qualified professionals to assess client needs and deliver the enhancements identified by their requirements. The team worked together as a joint team to accomplish the project objectives. Microsoft SureStep was leveraged as the project methodology to ensure that all requirements were document and the project was managed in a manner consistent with project management best practices. GAMP 5 is the methodology of choice leveraged for the FDA Validation Toolkit. All validation deliverables and test documentation was developed in a manner consistent with GAMP 5. The approach for this implementation was to migrate the legacy data from the existing systems and validate the new enhanced systems according to GAMP 5 and FDA validation guidelines.

Results

Impacts and outcomes

The FDA validation toolkit was used to streamline validation efforts. The templates and validation processes developed were used by the company to develop a corporate approach for validation and the test scripts were used to validate the system. All functionality and enhancements were delivered to the client as agreed.

Conclusions

The client acquired a new company and needed to leverage the validation documentation previously used and bring the new location online in a compliant manner. After the first successful implementation, the previous validation processes and documentation to validate the new location. In selecting Microsoft Dynamics AX 2009, the customer needed the confidence that the system could be validated in a compliant manner. In addition to the many features delivered by the integrated Microsoft Dynamics AX 2009 system, the customer achieved the following key business benefits:

Experienced Implementation and Validation Team

New eDHR/DMR Functionality

Field Service Engineering Enhancements

Reusable Validation Test Scripts

Advanced Project Management

Comprehensive ,Streamlined Validation Processes Leveraging The FDA Validation Toolkit

Validation Experience in Highly Regulated Industries

21 CFR Part 11 Compliance Built Into Microsoft Dynamics AX 2009